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2-(3-bromo-2-nitrophenyl)acetic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

400629-31-4

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400629-31-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 400629-31-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,0,6,2 and 9 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 400629-31:
(8*4)+(7*0)+(6*0)+(5*6)+(4*2)+(3*9)+(2*3)+(1*1)=104
104 % 10 = 4
So 400629-31-4 is a valid CAS Registry Number.

400629-31-4Relevant academic research and scientific papers

Synthesis and evaluation of new benzimidazole-based COX inhibitors: A naproxen-like interaction detected by STD-NMR

Carvalho, Luísa C. R.,Ribeiro, Daniela,Seixas, Raquel S. G. R.,Silva, Artur M. S.,Nave, Mariana,Martins, Ana C.,Erhardt, Stefan,Fernandes, Eduarda,Cabrita, Eurico J.,Marques, M. Manuel B.

, p. 49098 - 49109 (2015)

Non-steroidal anti-inflammatory drugs exert their pharmacological activity through inhibition of cyclooxygenase 1 and 2 (COX-1 and COX-2). Recent research suggests that a balanced inhibition of both COX-1 and COX-2 is the key to reduce the side-effects ex

A 3 - bromo -2 - nitrobenzaldehyde chemical synthesis method

-

, (2018/07/15)

The invention relates to a chemical synthesis method of 3-bromo-2-nitrobenzaldehyde. The chemical synthesis method is characterized by using 1,3-dibromo-2-nitrobenzene as a raw material and carrying out five-step reactions including substitution, decarboxylation, oxidation, reduction and hydroformylation, and comprises the following steps of adding 1,3-dibromo-2-nitrobenzene, dimethyl malonate and alkali to an organic solvent to react to prepare 2-(3-bromo-2-nitrobenzaldehyde)-dimethyl malonate; dissolving 2-(3-bromo-2-nitrobenzaldehyde)-dimethyl malonate obtained in the former step in a tetrahydrofuran or acetone solvent, and adding a hydrochloric acid solution to react to prepare 2-(3-bromo-2-nitrobenzaldehyde)-acetic acid; adding a sodium hydroxide water solution and potassium permanganate to react to obtain 3-bromo-2-nitrobenzoic acid; dissolving 3-bromo-2-nitrobenzoic acid in the tetrahydrofuran solvent, and adding borane tetrahydrofuran to react to obtain 3-bromo-2-nitrobenzyl alcohol; adding 3-bromo-2-nitrobenzyl alcohol to a dichloromethane or 1,2-dichloroethane solvent and adding manganese dioxide to react to prepare 3-bromo-2-nitrobenzaldehyde. The synthetic route has the advantages of low cost and high yield.

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