1-Bromo-2-naphthoic Acid - ≥98% , CAS No.20717-79-7

CAS: 20717-79-7 Cat. No.: B135350 Peso molecular: 251.08 Número EC: 243-984-9
Disponible para pedir
GRADE & PURITY ≥98%
Synonyms
1-(4-Fluorophenyl)-4-(4-hydroxy-4-p-tolylpiperidin-1-yl)butan-1-one | 6,10-diazatricyclo[7.4.0.02,7]trideca-1(9),2(7),3,5,10,12-hexaen-8-one | 27B | Maybridge4_002377 | 6-amino-5-(methylamino)-1-(phenylmethyl)pyrimidine-2,4-dione | 1-Bromo-naphthalene-2-c
Storage
Room temperature
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
200mg
B135350-200mg
5

9,90US$

14,90US$
Guardar 5,00 US$ (33.56%)
1g
B135350-1g
5

11,90US$

17,90US$
Guardar 6,00 US$ (33.52%)
5g
B135350-5g
6

34,90US$

52,90US$
Guardar 18,00 US$ (34.03%)
10g
B135350-10g
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.

56,90US$

85,90US$
Guardar 29,00 US$ (33.76%)
25g
B135350-25g
1

111,90US$

167,90US$
Guardar 56,00 US$ (33.35%)
100g
B135350-100g
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.

419,90US$

629,90US$
Guardar 210,00 US$ (33.34%)
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Why this grade

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

🌡

Storage & shipping

Room temperature Ships Normal 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.

📚

Literature proof

Cited in 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

Reactant involved in synthesis of: Binaphthyl-based amino acids and amino alcohols via domino coupling reactions and lactam ring opening of intermediates Benzimidazoles and benzimidazolequinone derivatives via cyclocondensation Axially chiral biaryls via Suzuki-Miyaura reactions Aryl ring-fused benzimidazolequinones via radical cyclization Probes for human cytochrome P450 enzymes Phananthridinone derivatives via domino coupling reactions

Specifications

Sinónimos
1-(4-Fluorophenyl)-4-(4-hydroxy-4-p-tolylpiperidin-1-yl)butan-1-one | 6, 10-diazatricyclo[7.4.0.02, 7]trideca-1(9), 2(7), 3, 5, 10, 12-hexaen-8-one | 27B | Maybridge4_002377 | 6-amino-5-(methylamino)-1-(phenylmethyl)pyrimidine-2, 4-dione | 1-Bromo-naphthalene-2-c
Especificaciones y pureza
≥98%
Condiciones de almacenamiento de almacenamiento
Room temperature
Enviado en
Normal
Pureza
≥98%
Nombres e identificadores
Pubchem Sid488186511
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488186511
Sonrisas canónicasC1=CC=C2C(=C1)C=CC(=C2Br)C(=O)O
IUPAC Name1-bromonaphthalene-2-carboxylic acid
InChIKeyVUVIRKAVBZITDO-UHFFFAOYSA-N
INCHI1S/C11H7BrO2/c12-10-8-4-2-1-3-7(8)5-6-9(10)11(13)14/h1-6H,(H,13,14)
Isómeros SMILES C1=CC=C2C(=C1)C=CC(=C2Br)C(=O)O
WGK Alemania 3
Peso molecular 251.08
Reaxy-Rn 2445031
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2445031&ln=

Documentation

📋 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
ClaseNaphthalenes
SubclassNaphthalenecarboxylic acids and derivatives
Intermediate Tree Nodes Not available
Direct ParentNaphthalenecarboxylic acids
Alternative Parents 1-carboxy-2-haloaromatic compounds  Aryl bromides  Vinylogous halides  Monocarboxylic acids and derivatives  Organooxygen compounds  Organobromides  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAromatic homopolycyclic compounds
Substituents 2-naphthalenecarboxylic acid - 1-carboxy-2-haloaromatic compound - Aryl halide - Aryl bromide - Vinylogous halide - Monocarboxylic acid or derivatives - Carboxylic acid - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organobromide - Organohalogen compound - Aromatic homopolycyclic compound
DescripciónThis compound belongs to the class of organic compounds known as naphthalenecarboxylic acids. These are compounds containing a naphthalene moiety, which bears a carboxylic acid group one or more positions. Naphthalene is a bicyclic compound that is made up of two fused benzene ring.
External Descriptors Not available
Estructura 3D
Modelo de Estructura Química Interactiva





Mecanismos de acción
Certificados (CoA, COO, BSE/TSE y tabla de análisis)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

6 results found

Lot NumberCertificate TypeFechaArticulo
F2207347Certificate of AnalysisDec 12, 2025 B135350
F2207348Certificate of AnalysisDec 12, 2025 B135350
F2207349Certificate of AnalysisDec 12, 2025 B135350
C23151120Certificate of AnalysisApr 01, 2023 B135350
H1731046Certificate of AnalysisFeb 09, 2023 B135350
C23151119Certificate of AnalysisJun 10, 2022 B135350
Propiedades químicas y físicas
Punto de fusión (°C)191 °C
Peso molecular251.080 g/mol
XLogP33.400
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count2
Rotatable Bond Count1
Exact Mass249.963 Da
Monoisotopic Mass249.963 Da
Topological Polar Surface Area37.300 Ų
Heavy Atom Count14
Formal Charge0
Complexity229.000
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
Citations of This Product
Referencias
1. Haoxiang Meng, Song Xue, Sihui Ding, Qing Wu, Zanhao Huang, Qi Zhang.  (2025)  Cyclodextrin-electrokinetic chromatography using Betaine:Urea, a deep eutectic solvent as the separation medium.  JOURNAL OF CHROMATOGRAPHY A,      [PMID:40505363] [10.1016/j.chroma.2025.466130]
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