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637041-67-9

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637041-67-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 637041-67-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,3,7,0,4 and 1 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 637041-67:
(8*6)+(7*3)+(6*7)+(5*0)+(4*4)+(3*1)+(2*6)+(1*7)=149
149 % 10 = 9
So 637041-67-9 is a valid CAS Registry Number.

637041-67-9SDS

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 Ethyl 3-amino-4-(tert-butylamino)benzoate

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:637041-67-9 SDS

637041-67-9Downstream Products

637041-67-9Relevant articles and documents

Microwave-assisted synthesis of sec/tert-butyl 2-arylbenzimidazoles and their unexpected antiproliferative activity towards ER negative breast cancer cells

Abdul Rahim, Aisyah Saad,Muhamad Salhimi, Salizawati,Arumugam, Natarajan,Pin, Lim Chung,Yee, Ng Shy,Muttiah, Nithya Niranjini,Keat, Wong Boon,Abd. Hamid, Shafida,Osman, Hasnah,Mat, Ishak B.

, p. 1255 - 1260 (2013/12/04)

A new series of N-sec/tert-butyl 2-arylbenzimidazole derivatives was synthesised in 85-96% yields within 2-3.5min by condensing ethyl 3-amino-4-butylamino benzoate with various substituted metabisulfite adducts of benzaldehyde under focused microwave irradiation. The benzimidazole analogues were characterised using 1H NMR, 13C NMR, high resolution MS and melting points. Evaluation of antiproliferative activity of the benzimidazole analogues against MCF-7 and MDA-MB-231 revealed several compounds with unexpected selective inhibitions of MDA-MB-231 in micromolar range. All analogues were found inactive towards MCF-7. The most potent inhibition against MDA-MB-231 human breast cancer cell line came from the unsubstituted 2-phenylbenzimidazole 10a.

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