RPW-24 - ≥98% , CAS No.1001625-82-6

Name: RPW-24 - ≥98% , CAS No.1001625-82-6
SKU: R412433
Availability: InStock

CAS: 1001625-82-6 Cat. No.: R412433 Formule: C₁₅H₁₃ClN₄ Poids moléculaire: 284.74 PubChem CID: 2227970

COA

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RPW-24 - CAS No(1001625-82-6) by Aladdin Scientific

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DISPONIBLE À COMMANDE

GRADE & PURITY ≥98%

Storage

Store at -20°C

Shipped In

Ice chest + Ice pads

Vue d’ensemble Specifications Noms et identifiants Documentation Advanced Data Taxonomic Classification Structure 3D Cibles associées (humaines) Cibles associées (non humaines) Mécanismes d'action Certificats (CoA, COO, BSE/TSE et tableau d'analyse) Propriétés chimiques et physiques Calculateurs de solution Avis

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Why this grade

≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Store at -20°C Ships Ice chest + Ice pads Check lot-specific COA for exact specifications.

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Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

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Literature proof

Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Vue d’ensemble

Information

RPW-24 protects C. elegans from bacterial infection by stimulating the host immune response of the nematode with antibacterial activity.

Specifications

Spécifications et pureté

≥98%

Mécanismes biochimiques et physiologiques

RPW-24 protects C. elegans from bacterial infection by stimulating the host immune response of the nematode with antibacterial activity.

Conditions de stockage de stockage

Store at -20°C

Expédié en

Ice chest + Ice pads

Ce produit nécessite l'expédition en chaîne froide. Les services terrestres et autres services économiques ne sont pas disponibles.

Type d'action

INHIBITOR

Pureté

≥98%

Noms et identifiants

Sourires canoniques

CC1=C(C=C(C=C1)NC2=NC3=CC=CC=C3C(=N2)N)Cl

IUPAC Name

2-N-(3-chloro-4-methylphenyl)quinazoline-2,4-diamine

InChIKey

LFMFPKKYRXFHHZ-UHFFFAOYSA-N

INCHI

1S/C15H13ClN4/c1-9-6-7-10(8-12(9)16)18-15-19-13-5-3-2-4-11(13)14(17)20-15/h2-8H,1H3,(H3,17,18,19,20)

Isomères SMILES

CC1=C(C=C(C=C1)NC2=NC3=CC=CC=C3C(=N2)N)Cl

PubChem CID

2227970

Poids moléculaire

284.74

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

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✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

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📊 Datasheet

Quick-reference summary of product specifications and applications.

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🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

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Advanced Data

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organoheterocyclic compounds
  - Classe Diazanaphthalenes
    - Subclass Benzodiazines
      - Level5 Quinazolines
        Level6 Quinazolinamines

Kingdom	Organic compounds
Superclass	Organoheterocyclic compounds
Classe	Diazanaphthalenes
Subclass	Benzodiazines
Intermediate Tree Nodes	Quinazolines
Direct Parent	Quinazolinamines
Alternative Parents	Aniline and substituted anilines Toluenes Chlorobenzenes Aminopyrimidines and derivatives Imidolactams Aryl chlorides Heteroaromatic compounds Secondary amines Azacyclic compounds Primary amines Organopnictogen compounds Organochlorides Hydrocarbon derivatives
Molecular Framework	Aromatic heteropolycyclic compounds
Substituents	Quinazolinamine - Aniline or substituted anilines - Aminopyrimidine - Chlorobenzene - Halobenzene - Toluene - Imidolactam - Benzenoid - Aryl chloride - Pyrimidine - Aryl halide - Monocyclic benzene moiety - Heteroaromatic compound - Secondary amine - Azacycle - Hydrocarbon derivative - Organohalogen compound - Amine - Organochloride - Organonitrogen compound - Organopnictogen compound - Primary amine - Organic nitrogen compound - Aromatic heteropolycyclic compound
Description	This compound belongs to the class of organic compounds known as quinazolinamines. These are heterocyclic aromatic compounds containing a quianazoline moiety substituted by one or more amine groups.
External Descriptors	substituted aniline - secondary amino compound - primary amino compound - monochlorobenzenes - quinazolines
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Structure 3D

Cibles associées (humaines)

KCNH2 Tclin HERG (29587 Activities)

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SLC2A1 Tchem Glucose transporter (14755 Activities)

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A498 (42825 Activities)

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ACHN (49357 Activities)

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CAKI-1 (44928 Activities)

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CCRF-CEM (65223 Activities)

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COLO 205 (50209 Activities)

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DU-145 (51482 Activities)

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Huh-7 (12904 Activities)

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KM12 (47707 Activities)

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M14 (47487 Activities)

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MCF7 (126967 Activities)

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MDA-MB-468 (9477 Activities)

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MOLT-4 (49676 Activities)

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MRC5 (9203 Activities)

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OVCAR-3 (48710 Activities)

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OVCAR-4 (44535 Activities)

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OVCAR-5 (45555 Activities)

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OVCAR-8 (47708 Activities)

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PC-3 (62116 Activities)

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RPMI-8226 (44974 Activities)

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RXF 393 (41971 Activities)

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SK-MEL-2 (46422 Activities)

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SK-MEL-28 (48833 Activities)

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SK-MEL-5 (47095 Activities)

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SK-OV-3 (52876 Activities)

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SN12C (47755 Activities)

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SNB-19 (46794 Activities)

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TK-10 (45540 Activities)

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U-251 (51189 Activities)

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UACC-257 (46019 Activities)

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UACC-62 (47335 Activities)

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UO-31 (46270 Activities)

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786-0 (47912 Activities)

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NCI/ADR-RES (33767 Activities)

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NCI-H322M (45589 Activities)

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HCT-116 (91556 Activities)

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HOP-92 (41141 Activities)

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HepG2 (196354 Activities)

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NCI-H460 (60772 Activities)

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SF-268 (49410 Activities)

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IGROV-1 (47897 Activities)

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HOP-62 (47048 Activities)

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MDA-MB-435 (38290 Activities)

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SNB-75 (44215 Activities)

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NCI-H23 (49055 Activities)

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NCI-H522 (44358 Activities)

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BT-549 (31254 Activities)

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SF-539 (44845 Activities)

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SR (39847 Activities)

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Cibles associées (non humaines)

Mycobacterium tuberculosis (203094 Activities)

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Saccharomyces cerevisiae (19171 Activities)

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Leishmania infantum (5912 Activities)

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Trypanosoma brucei brucei (13300 Activities)

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Entamoeba histolytica (2676 Activities)

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Cryptosporidium parvum (1150 Activities)

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Plasmodium falciparum (966862 Activities)

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Trypanosoma cruzi (99888 Activities)

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Toxoplasma gondii (4585 Activities)

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Plasmodium berghei (192651 Activities)

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Plasmodium yoelii (6656 Activities)

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Schistosoma mansoni (6170 Activities)

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Human immunodeficiency virus 1 (70413 Activities)

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Trypanosoma brucei rhodesiense (7991 Activities)

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ht1 Hexose transporter 1 (14071 Activities)

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pk7 Putative uncharacterized protein pk7 (469 Activities)

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CDPK1 Calcium-dependent protein kinase 1 (793 Activities)

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Onchocerca lienalis (1836 Activities)

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CDPK4 Calcium-dependent protein kinase 4 (464 Activities)

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PK6 Cdk-related protein kinase 6 (400 Activities)

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map-2 Mitogen-activated protein kinase (400 Activities)

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proRS Proline--tRNA ligase (401 Activities)

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Lysine--tRNA ligase (69390 Activities)

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Mécanismes d'action

Certificats (CoA, COO, BSE/TSE et tableau d'analyse)

C of A & Other Certificates(BSE/TSE, COO):

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4 results found

Lot Number	Certificate Type	Date	Article
I2617629	Certificate of Analysis	Apr 16, 2026	R412433
I2617630	Certificate of Analysis	Apr 16, 2026	R412433
I2617631	Certificate of Analysis	Apr 16, 2026	R412433
I2617632	Certificate of Analysis	Apr 16, 2026	R412433

Propriétés chimiques et physiques

Poids moléculaire	284.740 g/mol
XLogP3	4.200
Hydrogen Bond Donor Count	2
Hydrogen Bond Acceptor Count	4
Rotatable Bond Count	2
Exact Mass	284.083 Da
Monoisotopic Mass	284.083 Da
Topological Polar Surface Area	63.800 Å²
Heavy Atom Count	20
Formal Charge	0
Complexity	327.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	0
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	1

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RPW-24 - ≥98% , CAS No.1001625-82-6

Storage & shipping

Quality documents

Literature proof

Vue d’ensemble

Specifications

Documentation

📋 Safety Data Sheet (SDS)

✅ Certificate of Analysis (COA)

📊 Datasheet

🔬 Specification Sheet

Advanced Data

Molarity Calculator

Dilution Calculator

Reconstitution Calculator

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