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4-Hydroxy-3-methyl-5-nitrobenzaldehyde is an organic compound with the chemical formula C8H7NO4. It is a yellow crystalline solid that is soluble in organic solvents such as ethanol and acetone. 4-hydroxy-3-methyl-5-nitrobenzaldehyde is characterized by the presence of a hydroxyl group (-OH) at the 4th carbon, a methyl group (-CH3) at the 3rd carbon, and a nitro group (-NO2) at the 5th carbon of the benzene ring. The aldehyde group (-CHO) is attached to the 1st carbon. It is used as an intermediate in the synthesis of various pharmaceuticals, dyes, and other organic compounds. Due to its reactivity, it is important to handle 4-hydroxy-3-methyl-5-nitrobenzaldehyde with care, as it may be sensitive to light, heat, and moisture.

54674-91-8

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54674-91-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 54674-91-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,6,7 and 4 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 54674-91:
(7*5)+(6*4)+(5*6)+(4*7)+(3*4)+(2*9)+(1*1)=148
148 % 10 = 8
So 54674-91-8 is a valid CAS Registry Number.

54674-91-8Relevant academic research and scientific papers

The pyrazole derivative or its salt in a pharmaceutical composition containing them

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Paragraph 0081; 0109, (2017/01/26)

PROBLEM TO BE SOLVED: To provide a novel compound and a pharmaceutical composition useful for treatment and/or prevention of HIV virus infections.SOLUTION: Provided is a pyrazole derivative represented by the general formula (I) or a salt thereof (in the

Structure-activity relationship study of phenylpyrazole derivatives as a novel class of anti-HIV agents

Mizuhara, Tsukasa,Kato, Takayuki,Hirai, Atsushi,Kurihara, Hideki,Shimada, Yasuhiro,Taniguchi, Masahiko,Maeta, Hideki,Togami, Hiroaki,Shimura, Kazuya,Matsuoka, Masao,Okazaki, Shiho,Takeuchi, Tomoki,Ohno, Hiroaki,Oishi, Shinya,Fujii, Nobutaka

, p. 4557 - 4561 (2013/08/23)

The structure-activity relationship of phenylpyrazole derivative 1 was investigated for the development of novel anti-HIV agents. Initial efforts revealed that the diazenyl group can be replaced by an aminomethylene group. In addition, we synthesized various derivatives by the reductive amination of benzaldehydes with 5-aminopyrazoles and carried out parallel structural optimization on the benzyl group and the pyrazole ring. This optimization led to a six-fold more potent derivative 32j than the lead compound 1, and this derivative has a 3′,4′-dichloro-(1,1′-biphenyl)-3-yl group.

Highly practical and cost-efficient synthesis of telmisartan: An antihypertensive drug

Wang, Ping,Zheng, Guo-Jun,Wang, Ya-Ping,Wang, Xiang-Jing,Wei, He-Geng,Xiang, Wen-Sheng

experimental part, p. 2509 - 2512 (2012/04/11)

A novel and cost-efficient strategy for synthesis of an antihypertensive drug telmisartan, a substituted bis-benzimidazole derivative, is described. The key strategy is the construction of bis-benzimidazole 4 by reductive cyclization of o-nitroanilines 11 with butyl aldehyde and cyclocondensation of aromatic aldehydes 9 with o-phenylenediamine, then N-alkylation is allowed to give the target compound telmisartan after hydrolysis. The simple operation and workup procedure, along with the low production costs, make it suitable for industrial production and will benefits those with cardiovascular disease.

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