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316155-87-0

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316155-87-0 Usage

General Description

1,7-Naphthyridine-2-carboxylic acid is a chemical compound with the molecular formula C9H5NO2. It is a heterocyclic compound containing both a naphthyridine ring and a carboxylic acid group. 1,7-Naphthyridine-2-carboxylic acid is used in the pharmaceutical industry as a building block for the synthesis of various bioactive molecules. It is also utilized in the field of medicinal chemistry for the design and development of new drug candidates. Additionally, 1,7-Naphthyridine-2-carboxylic acid has been studied for its potential biological activities, including its antibacterial and anticancer properties. Overall, this compound plays a crucial role in the development of new drugs and therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 316155-87-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,1,6,1,5 and 5 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 316155-87:
(8*3)+(7*1)+(6*6)+(5*1)+(4*5)+(3*5)+(2*8)+(1*7)=130
130 % 10 = 0
So 316155-87-0 is a valid CAS Registry Number.

316155-87-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,7-Naphthyridine-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names -

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:316155-87-0 SDS

316155-87-0Relevant articles and documents

Synthesis and regioselective alkylation of 1,6- and 1,7-naphthyridines

Colandrea,Naylor

, p. 8053 - 8057 (2007/10/03)

A regioselective alkylation of naphthyridines 4a-d, through the action of ethylchloroformate and benzylstannane 5, afforded the benzyl substituted dihydronaphthyridines 3a-d. These key intermediates 3a-d were transformed into the desired targets 2a-d in seven steps. (C) 2000 Elsevier Science Ltd.

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