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79979-69-4

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79979-69-4 Usage

General Description

2-Amino-1-naphthoic acid is a chemical compound with the molecular formula C11H9NO2. It is classified as an aromatic amine and is commonly used in the synthesis of dyes and pharmaceuticals. It is a derivative of 1-aminonaphthalene and is often a key intermediate in the production of various organic compounds. The compound is a yellow crystalline solid that is sparingly soluble in water and soluble in most organic solvents. It is an important building block in organic chemistry and is utilized in the production of various products including medicines, dyes, and pigments.

Check Digit Verification of cas no

The CAS Registry Mumber 79979-69-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,9,7 and 9 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 79979-69:
(7*7)+(6*9)+(5*9)+(4*7)+(3*9)+(2*6)+(1*9)=224
224 % 10 = 4
So 79979-69-4 is a valid CAS Registry Number.
InChI:InChI=1S/C11H9NO2/c12-9-6-5-7-3-1-2-4-8(7)10(9)11(13)14/h1-6H,12H2,(H,13,14)

79979-69-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Aminonaphthalene-1-carboxylic acid

1.2 Other means of identification

Product number -
Other names 2-AMINO-1-NAPHTHOIC 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:79979-69-4 SDS

79979-69-4Relevant articles and documents

Development of sulfonamide compounds as potent methionine aminopeptidase type II inhibitors with antiproliferative properties

Kawai, Megumi,BaMaung, Nwe Y.,Fidanze, Steve D.,Erickson, Scott A.,Tedrow, Jason S.,Sanders, William J.,Vasudevan, Anil,Park, Chang,Hutchins, Charles,Comess, Kenneth M.,Kalvin, Douglas,Wang, Jieyi,Zhang, Qian,Lou, Pingping,Tucker-Garcia, Lora,Bouska, Jennifer,Bell, Randy L.,Lesniewski, Richard,Henkin, Jack,Sheppard, George S.

, p. 3574 - 3577 (2007/10/03)

We have screened molecules for inhibition of MetAP2 as a novel approach toward antiangiogenesis and anticancer therapy using affinity selection/mass spectrometry (ASMS) employing MetAP2 loaded with Mn2+ as the active site metal. After a series

Degradation of Reed's Base and Combes' Base

Singh, Prem Narayan,Sinha, Girish Kumar,Singh, Nityanand

, p. 874 - 876 (2007/10/02)

Synthesis of 1,2,3,4-tetrahydro derivatives of Reed's base and its complete degradation to 2-amino-1-naphthoic acid are described.Similarly synthesis of 1,2,3,4-tetrahydro-2,4-dimethyl-6,7-benzoquinoline (Combes' base) and its complete degradation to 2-amino-3-naphthoic acid is also described.This constitutes an evidence that Reed's base is angular while Combes' base is linear.

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