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496925-70-3

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496925-70-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 496925-70-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,9,6,9,2 and 5 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 496925-70:
(8*4)+(7*9)+(6*6)+(5*9)+(4*2)+(3*5)+(2*7)+(1*0)=213
213 % 10 = 3
So 496925-70-3 is a valid CAS Registry Number.

496925-70-3SDS

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 5-formyl-2-methylthio-1-(4-nitrobenzyl) imidazole

1.2 Other means of identification

Product number -
Other names 2-Methylsulfanyl-3-(4-nitro-benzyl)-3H-imidazole-4-carbaldehyde

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:496925-70-3 SDS

496925-70-3Downstream Products

496925-70-3Relevant articles and documents

Synthesis and calcium antagonist activity of new 1,4-dihydropyridines containing nitrobenzylimidazolyl substituent in ginea-pig ileal smooth muscle

Zarghi,Derakhshandeh,Roshanzamir,Jorjani,Rastegar,Varmazyari,Shafiee

, p. 15 - 20 (2007/10/03)

New alkyl ester analogues of nifedipine, in which the ortho-nitrophenyl group of position 4 is replaced by 1-(4-nitrobenzyl)-5-imidazolyl or 2-methylthio-1-(4-nitrobenzyl)-5-imidazolyl substituent, were synthesized and evaluated as calcium-channel antagonists using the electrically induced contraction of guinea-pig ileal longitudinal smooth muscle. Our results demonstrate that all compounds inhibited the contractile response of guinea-pig ileum to electrical stimulation and the IC50 value of the most potent compounds 6a and 6f were significantly lower than that of nifedipine. Therefore, they are more potent than nifedipine.

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