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N-benzoyl-α-phenylthioglycine methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

25389-49-5

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25389-49-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 25389-49-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,3,8 and 9 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 25389-49:
(7*2)+(6*5)+(5*3)+(4*8)+(3*9)+(2*4)+(1*9)=135
135 % 10 = 5
So 25389-49-5 is a valid CAS Registry Number.

25389-49-5Downstream Products

25389-49-5Relevant academic research and scientific papers

One-pot regioselective synthesis of n-benzoyl 2-amino-3,4-dihydro-3-oxo-2h- 1,4-benzothiazi nes

Mabrouk,Elachqar,Alami,Hallaoui,Hajji

experimental part, p. 1249 - 1255 (2011/10/11)

A protocol for regioselective one-pot synthesis of 2-amino-3,4-dihydro-3- oxo-2H-1, 4-benzothiazmes has been developed. Starting from commercially available 2-aminothiophenols a basemediated regioselective S-alkylation took place with methyl α-azido glyci

Synthesis of unnatural amino acids from serine derivatives by β-fragmentation of primary alkoxyl radicals

Boto, Alicia,Gallardo, Juan A.,Hernandez, Dacil,Hernandez, Rosendo

, p. 7260 - 7269 (2008/02/11)

(Chemical Equation Presented) The fragmentation of primary alkoxyl radicals has been scarcely used in synthesis since other competing processes (such as oxidation or hydrogen abstraction) usually predominate. However, when serine derivatives were used as

Reactions of α-Substituted Glycine Derivatives with Stannanes in the Presence of Disulfides

Easton, Christopher J.,Peters, Steven C.

, p. 859 - 868 (2007/10/02)

Reactions of α-bromo-, α-benzoyloxy- and α-methoxy-substituted glycine derivatives with stannanes afforded the corresponding α-centred glycinyl radical, which reacted with di-t-butyl disulfide and diphenyl disulfide by homolytic substitution to give the corresponding α-t-butylthio- and α-phenylthio-substituted glycine derivatives, respectively.The glycinyl radical reacted with dibenzyl disulfide by displacement of benzyl radical to give a mixed disulfide, which was subsequently reduced to the corresponding α-benzylthio-substituted glycine derivative.In related reactions of a cystine derivative the corresponding S-glycinylcysteine derivative was produced, indicating that, while the chemical integrity of disulfide bonds in cystine derivatives is likely to be affected in radical reactions of peptides, the reactions are suitable for exploitation in the synthesis of cross-linked amino acid derivatives.

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