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659736-91-1

2-AMINO-1,2,3,4-TETRAHYDRO-6-BROMO-2-NAPHTHALENE CARBOXYLIC ACID is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 659736-91-1 Structure

  • Basic information

    1. Product Name: 2-AMINO-1,2,3,4-TETRAHYDRO-6-BROMO-2-NAPHTHALENE CARBOXYLIC ACID
    2. Synonyms: 2-AMINO-1,2,3,4-TETRAHYDRO-6-BROMO-2-NAPHTHALENE CARBOXYLIC ACID;2-Amino-1,2,3,4tetrahydro-6-bromo-2-naphtalene carboxylic acid, 90 %;2-Amino-1,2,3,4-tetrahydro-6-bromo-2-naphtalene carboxylic acid
    3. CAS NO:659736-91-1
    4. Molecular Formula: C11H12BrNO2
    5. Molecular Weight: 270.12
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 659736-91-1.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-AMINO-1,2,3,4-TETRAHYDRO-6-BROMO-2-NAPHTHALENE CARBOXYLIC ACID(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-AMINO-1,2,3,4-TETRAHYDRO-6-BROMO-2-NAPHTHALENE CARBOXYLIC ACID(659736-91-1)
    11. EPA Substance Registry System: 2-AMINO-1,2,3,4-TETRAHYDRO-6-BROMO-2-NAPHTHALENE CARBOXYLIC ACID(659736-91-1)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 659736-91-1(Hazardous Substances Data)

659736-91-1 Usage

Structure

Contains a bromine atom and an amino group; derivative of 2-naphthoic acid

Usage

Pharmaceutical Industry: Intermediate for synthesizing various organic compounds, including potential drug candidates.
Medicinal Chemistry Research: Suitable for research and drug discovery due to its structure and properties.
Other Industrial Applications: Possibly used in manufacturing dyes and pigments.

Check Digit Verification of cas no

The CAS Registry Mumber 659736-91-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,5,9,7,3 and 6 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 659736-91:
(8*6)+(7*5)+(6*9)+(5*7)+(4*3)+(3*6)+(2*9)+(1*1)=221
221 % 10 = 1
So 659736-91-1 is a valid CAS Registry Number.

659736-91-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-amino-6-bromo-3,4-dihydro-1H-naphthalene-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names 2-AMINO-1,2,3,4-TETRAHYDRO-6-BROMO-2-NAPHTHALENE CARBOXYLIC ACID

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:659736-91-1 SDS

659736-91-1Relevant articles and documents

Synthesis of α,α-disubstituted 4-phosphonophenylalanine analogues as conformationally-constrained phosphotyrosyl mimetics

Oishi, Shinya,Kang, Sang-Uk,Liu, Hongpeng,Zhang, Manchao,Yang, Dajun,Deschamps, Jeffrey R.,Burke Jr., Terrence R.

, p. 2971 - 2977 (2007/10/03)

Syntheses of N-Boc (S)-4-(diethylphosphono)-(α-methyl)phenylalanine [Boc-(α-Me)Phe(4-PO3Et2)-OH] (9) and N-Boc (S)-2-amino-6-(diethylphosphono)tetralin-2-carboxylic acid [Boc-Atc(6-PO 3Et2)-OH] (18) are reported

Structure-activity relationship of linear peptide Bu-His-DPhe-Arg-Trp-Gly-NH2 at the human melanocortin-1 and -4 receptors: Histidine substitution

Cheung, Adrian Wai-Hing,Danho, Waleed,Swistok, Joseph,Qi, Lida,Kurylko, Grazyna,Rowan, Karen,Yeon, Mitch,Franco, Lucia,Chu, Xin-Jie,Chen, Li,Yagaloff, Keith

, p. 133 - 137 (2007/10/03)

Systematic substitution of His6 residue using non-selective hMC4R pentapeptide agonist (Bu-His6-DPhe7-Arg8-Trp9-Gly 10-NH2) as the template led to the identification of Bu-Atcsu

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