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63678-16-0

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63678-16-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 63678-16-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,6,7 and 8 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 63678-16:
(7*6)+(6*3)+(5*6)+(4*7)+(3*8)+(2*1)+(1*6)=150
150 % 10 = 0
So 63678-16-0 is a valid CAS Registry Number.

63678-16-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N-phenyl-1H-imidazole-2-carboxamide

1.2 Other means of identification

Product number -
Other names HMS1442I22

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:63678-16-0 SDS

63678-16-0Relevant articles and documents

HETEROCYCLIC CARBOXYLIC ACID AMIDE LIGAND AND APPLICATIONS THEREOF IN COPPER CATALYZED COUPLING REACTION OF ARYL HALOGENO SUBSTITUTE

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Paragraph 0253, (2019/05/15)

Provided are a heterocyclic carboxylic acid amide ligand and applications thereof in a copper catalyzed coupling reaction. Specifically, provided are uses of a compound represented by formula (I), definitions of radical groups being described in the specifications. The compound represented by formula (I) can be used as the ligand in the copper catalyzed coupling reaction of the aryl halogeno substitute, and is used or catalyzing the coupling reaction for forming the aryl halogeno substitute having C—N, C—O, C—S and other bonds.

PYRROLOTRIAZINONE DERIVATIVES AS PI3K INHIBITORS

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Page/Page column 118-119, (2012/11/13)

New pyrrolotriazinone derivatives having the chemical structure of formula (I) are disclosed; as well as process for their preparation, pharmaceutical compositions comprising them and their use in therapy as inhibitors of Phosphoinositide 3-Kinases (PI3Ks).

Method for producing a 3-oxo-propionic acid amide compound and substituted acetyl compound used therein

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, (2008/06/13)

There is disclosed (A) a method for producing a 3-oxopropionic acid amide compound, comprising reacting urethanes with substituted or unsubstituted acetyl compounds in the presence of a base; and (B) a substituted acetyl compound represented by formula (I

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