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Quinoline, 2,6-dimethoxy-3-(phenylmethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

918518-76-0

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918518-76-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 918518-76-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,8,5,1 and 8 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 918518-76:
(8*9)+(7*1)+(6*8)+(5*5)+(4*1)+(3*8)+(2*7)+(1*6)=200
200 % 10 = 0
So 918518-76-0 is a valid CAS Registry Number.

918518-76-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-benzyl-2,6-dimethoxyquinoline

1.2 Other means of identification

Product number -
Other names Quinoline,2,6-dimethoxy-3-(phenylmethyl)

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:918518-76-0 SDS

918518-76-0Downstream Products

918518-76-0Relevant articles and documents

QUINOLINE DERIVATIVES AS ANTIBACTERIAL AGENTS

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Page/Page column 31, (2010/11/25)

Use of a compound for the manufacture of a medicament for the treatment of a bacterial infection provided that the bacterial infection is other than a Mycobacterial infection, said compound being a compound of formula (Ia) or (Ib) a pharmaceutically acceptable acid or base addition salt thereof, a stereochemically isomeric form thereof, a tautomeric form thereof or a N-oxide form thereof. Several of these compounds are also claimed as such. Further the combination of the above compounds with other antibacterial agents is described

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