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862845-69-0

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862845-69-0 Usage

General Description

BENZAMIDE, N-[7-(CHLOROMETHYL)-1-ISOQUINOLINYL]- is a chemical compound that belongs to the benzamide and isoquinoline families. It is an organic compound with the molecular formula C20H15ClN2O and a molecular weight of 340.8 g/mol. This chemical is used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It contains a benzene ring and an amide group, as well as a chlorine-substituted isoquinoline ring. Its precise uses and applications may vary depending on the specific industry and context in which it is employed.

Check Digit Verification of cas no

The CAS Registry Mumber 862845-69-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,2,8,4 and 5 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 862845-69:
(8*8)+(7*6)+(6*2)+(5*8)+(4*4)+(3*5)+(2*6)+(1*9)=210
210 % 10 = 0
So 862845-69-0 is a valid CAS Registry Number.
InChI:InChI=1S/C17H13ClN2O/c18-11-12-6-7-13-8-9-19-16(15(13)10-12)20-17(21)14-4-2-1-3-5-14/h1-10H,11H2,(H,19,20,21)

862845-69-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[7-(chloromethyl)isoquinolin-1-yl]benzamide

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:862845-69-0 SDS

862845-69-0Relevant articles and documents

Design, synthesis and testing of amino-bicycloaryl based orally bioavailable thrombin inhibitors

Rewinkel,Lucas,Smit,Noach,Van Dinther,Rood,Jenneboer,Van Boeckel

, p. 2837 - 2842 (2007/10/03)

Replacement of the highly basic benzamidine moiety with moderate basic amino-bicycloaryl moieties in a series of thrombin inhibitors related to NAPAMP provided potent enzyme inhibition and significant improvements in membrane transport and oral bioavailability.

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