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866946-42-1

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866946-42-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 866946-42-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,6,9,4 and 6 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 866946-42:
(8*8)+(7*6)+(6*6)+(5*9)+(4*4)+(3*6)+(2*4)+(1*2)=231
231 % 10 = 1
So 866946-42-1 is a valid CAS Registry Number.

866946-42-1SDS

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 2-(4-aminomethylphenyl)benzamide

1.2 Other means of identification

Product number -
Other names 4-aminomethyl-1,1'-biphenyl-2'-carboxamide

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:866946-42-1 SDS

866946-42-1Relevant articles and documents

A novel approach for the conversion of primary amides into tetrazoles by using tributyltin chloride and sodium azide in the presence of DMF

Prasada Rao, Korrapati V. V.,Dandala, Ramesh,Handa, Vijay K.,Subramanyeswara Rao, Inti V.,Rani, Ananta,Shivashankar, Sripelly,Naidu, Andra

, p. 1289 - 1293 (2008/02/07)

A novel and efficient one-pot synthesis of tetrazole derivatives such as Irbesartan and its analogues has been described from the primary acid amide derivatives. Thus 2-alkyl-3-[p-(o-ami-dophenyl (benzyl]-1.3-diazaspiro[4.4]non- 1-en-4-one derivatives or 4-[α-(acylamino)cyclopentamidomethyl]-2′- carboxamidobiphenyl derivatives were treated with tributyltin chloride and sodium azide in o-xylene in the presence of DMF to afford irbesartan and its analogues without generation of nitriles. The synthesis of these new starting materials is also described, and two of the derivatives have been used as new intermediates in the preparation of irbesartan. Georg Thieme Verlag Stuttgart.

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