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(4,5-dimethoxy-2-nitrophenyl)(methyl)sulfane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

30058-45-8

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30058-45-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 30058-45-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,0,5 and 8 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 30058-45:
(7*3)+(6*0)+(5*0)+(4*5)+(3*8)+(2*4)+(1*5)=78
78 % 10 = 8
So 30058-45-8 is a valid CAS Registry Number.

30058-45-8Relevant academic research and scientific papers

Palladium-catalyzed decarboxylative methylthiolation of aromatic carboxylic acids by using DMSO as the sulfurizing reagent

Fu, Zhengjiang,Li, Zhaojie,Xiong, Qiheng,Cai, Hu

, p. 7798 - 7802 (2014)

By using simple and readily available DMSO as a convenient and environmentally friendly source of sulfur, a practical approach for the Pd-catalyzed decarboxylative methylthiolation of 2-nitrobenzoic acids was developed. A range of substituents on the aryl group of the ortho-nitrobenzoic acid were compatible with this process.

Copper-catalyzed decarboxylative methylthiolation of aromatic carboxylate salts with DMSO

Hu, Liang,Wang, Dadian,Chen, Xiang,Yu, Lin,Yu, Yongqi,Tan, Ze,Zhu, Gangguo

supporting information, p. 5674 - 5679 (2017/07/22)

A novel copper-catalyzed decarboxylative methylthiolation of arenecarboxylate salts has been realized using DMSO as the methylthiolation source. Various potassium aryl carboxylates underwent decarboxylative methylthiolation under air to furnish the corresponding aryl methyl thioethers in moderate to excellent yields. The reaction tolerated a wide variety of functional groups. Notably, the synthesis of ethylthioethers was also successfully achieved directly from diethyl sulfoxide under similar reaction conditions.

Synthesis and blood pressure lowering activity of 3-(substituted-amino)-1,2,4-benzothiadazine 1-oxide derivatives

Dillard,Yen,Stark,Pavey

, p. 717 - 722 (2007/10/02)

A series of (substituted amino)-1,2,4-benzothiadiazine 1-oxides has been synthesized and most members of the series have been shown to have blood-pressure lowering effects in normotensive rabbits and in spontaneously hypertensive rats. The most active member of the series was 3-[4-(2-furoyl)-1-piperazinyl]-6,7-dimethoxy-1-methyl-1H-1,2,4-benzothiadiazine 1-oxide hydrochloride. This compound in animal tests was equipotent to the known antihypertensive Prazosin.

1,3-Dialkyl-6,7-methoxy-1H-1,2,4-benzothiadiazine-1-oxides

-

, (2008/06/13)

1,3-Dialkyl-6,7-methoxy-1H-1,2,4-benzothiadiazine-1-oxides, useful as hypotensive agents.

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