Ftaxilide - 10mM in DMSO , CAS No.19368-18-4

CAS: 19368-18-4 Cat. No.: F422365 Formula: C16H15NO3 Peso molecolare: 269.3 Numero EC: 666-316-1
Disponibile su ordine
GRADE & PURITY 10mM in DMSO
Synonyms
4,4'-Thiobis(2-tert-butyl-6-methylphenol) | FTAXILIDE [INN] | Tox21_111986 | AKOS001678089 | Salicylic acid, 5-nitro- | 1-(Diisopropylamino)-2-chloroethane | lactobionate | SR-01000253137-3 | Ftaxilidum | Ftaxilide | Phenol, 2,4-di-tert-butyl- | Yoshinox
Storage
Store at -80°C
Shipped In
Dry ice packs + Cold packs
★
Size
Germania (EU)
USA*
Price
Qty
1ml
F422365-1ml
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1 Disponibile

51,11€

60,65€
Salva 9,55 € (15.74%)
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Why this grade

10mM in DMSO for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at -80°C Ships Dry ice packs + Cold packs Check lot-specific COA for exact specifications.

📋

Quality documents

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

📚

Literature proof

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

Panoramica

Information

Ftaxilide Ftaxilide is a novel antituberculosis agent.

Specifications

Sinonimi
4,4'-Thiobis(2-tert-butyl-6-methylphenol) | FTAXILIDE [INN] | Tox21_111986 | AKOS001678089 | Salicylic acid, 5-nitro- | 1-(Diisopropylamino)-2-chloroethane | lactobionate | SR-01000253137-3 | Ftaxilidum | Ftaxilide | Phenol, 2,4-di-tert-butyl- | Yoshinox
Specifiche e purezza
10mM in DMSO
Meccanismi biochimici e fisiologici
Ftaxilide is a novel antituberculosis agent.
Condizioni di conservazione di stoccaggio
Store at -80°C
Spedito in
Dry ice packs + Cold packs
Questo prodotto richiede spedizione a catena fredda. I servizi di terra e altri servizi economici non sono disponibili.
Tipo di azione
INHIBITOR
Proprietà del prodotto
ALogP3.216
hba_count2
Conteggio HBD1
Legame rotabile3
Nomi e identificatori
Pubchem Sid528764559
Sorrisi canoniciCC1=C(C(=CC=C1)C)NC(=O)C2=CC=CC=C2C(=O)O
IUPAC Name2-[(2,6-dimethylphenyl)carbamoyl]benzoic acid
InChIKeyLLECMGGNFBKPRH-UHFFFAOYSA-N
INCHI1S/C16H15NO3/c1-10-6-5-7-11(2)14(10)17-15(18)12-8-3-4-9-13(12)16(19)20/h3-9H,1-2H3,(H,17,18)(H,19,20)
Isomeri SMILES CC1=C(C(=CC=C1)C)NC(=O)C2=CC=CC=C2C(=O)O
Peso molecolare 269.3
Reaxy-Rn 2659992
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2659992&ln=

Documentazione

📋 Safety Data Sheet (SDS)

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

Download SDS →

✅ Certificate of Analysis (COA)

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

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassBenzenoids
ClasseBenzene and substituted derivatives
SubclassAnilides
Intermediate Tree Nodes Aromatic anilides
Direct ParentBenzanilides
Alternative Parents Benzoic acids  Benzamides  m-Xylenes  Benzoyl derivatives  Secondary carboxylic acid amides  Monocarboxylic acids and derivatives  Carboxylic acids  Organopnictogen compounds  Organooxygen compounds  Organonitrogen compounds  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAromatic homomonocyclic compounds
Substituents Benzanilide - Benzamide - Benzoic acid or derivatives - Benzoic acid - Benzoyl - M-xylene - Xylene - Carboxamide group - Secondary carboxylic acid amide - Monocarboxylic acid or derivatives - Carboxylic acid - Carboxylic acid derivative - Organooxygen compound - Organonitrogen compound - Organic oxide - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Hydrocarbon derivative - Aromatic homomonocyclic compound
DescrizioneThis compound belongs to the class of organic compounds known as benzanilides. These are aromatic compounds containing an anilide group in which the carboxamide group is substituted with a benzene ring. They have the general structure RNC(=O)R', where R,R'= benzene.
External Descriptors Not available
Struttura 3D
Modello di struttura chimica interattiva





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Meccanismi d'azione
Certificati (CoA, COO, BSE/TSE e tabella di analisi)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Proprietà chimiche e fisiche
DMSO (mg/mL) Solubilità massima54
DMSO (mM) Solubilità massima200.519866320089
Acqua (mg/mL) Solubilità massima<1
Peso molecolare269.290 g/mol
XLogP33.000
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count3
Rotatable Bond Count3
Exact Mass269.105 Da
Monoisotopic Mass269.105 Da
Topological Polar Surface Area66.400 Ų
Heavy Atom Count20
Formal Charge0
Complexity359.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Calcolatori di soluzioni
Recensioni

Recensioni dei clienti

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