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(4-Methoxy-phenyl)-dithiocarbamic acid 4-bromo-benzyl ester is a complex organic compound with the chemical formula C15H14BrNOS2. It is a derivative of dithiocarbamic acid, featuring a 4-methoxy-phenyl group and a 4-bromo-benzyl ester group. (4-Methoxy-phenyl)-dithiocarbamic acid 4-bromo-benzyl ester is characterized by its potential applications in chemical research and synthesis, particularly in the development of agrochemicals and pharmaceuticals. The presence of the bromine atom and the methoxy group on the phenyl ring contribute to its unique chemical properties and reactivity. The compound's structure allows for various functional group transformations and reactions, making it a valuable intermediate in organic synthesis.

3153-16-0

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  • (4-Methoxy-phenyl)-dithiocarbamic acid 4-bromo-benzyl ester

    Cas No: 3153-16-0

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3153-16-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3153-16-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,5 and 3 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3153-16:
(6*3)+(5*1)+(4*5)+(3*3)+(2*1)+(1*6)=60
60 % 10 = 0
So 3153-16-0 is a valid CAS Registry Number.

3153-16-0Downstream Products

3153-16-0Relevant articles and documents

Efficient, straightforward, catalyst-free synthesis of medicinally important S-alkyl/benzyl dithiocarbamates under green conditions

Asadipour, Ali,Shams, Zeynab,Eskandari, Khalil,Moshafi, Mohammad-Hassan,Faghih-Mirzaei, Ehsan,Pourshojaei, Yaghoub

, p. 1295 - 1304 (2018)

Green synthesis of some novel dithiocarbamate derivatives substituted by aliphatic and aromatic groups as potentially interesting, medicinally important organic compounds via efficient one-pot, catalyst-free reaction is described. In this reaction, dithiocarbamate derivatives are obtained from condensation reaction between primary or secondary amines, carbon disulfide, and alkyl or benzyl halides in one pot and ethanol–aqueous medium. Among aliphatic and aromatic amines, the results generally show that reaction of aliphatic amines with alkyl or benzyl halides led to desired products in highest yields. Also, among aliphatic amines, those which reacted with benzyl halides showed better yields than those that reacted with alkyl halides. Use of environmentally benign solvents is one of the advantages of this procedure. Also, obtaining products in good yield via catalyst-free reaction using a facile, inexpensive, and practical approach can be considered other advantages of this procedure. Target products are very important compounds, because their analogs have been applied in pharmaceutical, chemical, and rubber industries.

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