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DL-Methionine, N-[(phenylmethoxy)carbonyl]-, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

83972-33-2

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83972-33-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 83972-33-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,9,7 and 2 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 83972-33:
(7*8)+(6*3)+(5*9)+(4*7)+(3*2)+(2*3)+(1*3)=162
162 % 10 = 2
So 83972-33-2 is a valid CAS Registry Number.

83972-33-2Relevant academic research and scientific papers

Chemoselective synthesis of carbamates using CO2 as carbon source

Riemer, Daniel,Hirapara, Pradipbhai,Das, Shoubhik

, p. 1916 - 1920 (2018/08/17)

Synthesis of carbamates directly from amines using CO2 as the carbon source is a straightforward and sustainable approach. Herein, we describe a highly effective and chemoselective methodology for the synthesis of carbamates at room temperature and atmosp

Structure and Stereochemistry of Three Phytotoxins, Syringomycin, Syringotoxin and Syringostatin, Produced by Pseudomonas syringae pv. syringae

Fukuchi, Naoyuka,Isogai, Akira,Nakayama, Jiro,Takayama, Seiji,Yamashita, Shuichi,et al.

, p. 1149 - 1158 (2007/10/02)

The structures of two phytotoxins, syringomycin and syringotoxin, produced by Pseudomonas syringae pv. syringae, were determined.Several amino acid residues of syringomycin were different from those in the syringostatins.Syringotoxin B proved to be syringostatin A.The three kinds of phytotoxins showed close structural similarity, and the stereochemistry of their components was deduced and compared.

SELECTIVE TRANSFORMATION OF N-t-BUTOXYCARBONYL GROUP INTO N-ALKOXYCARBONYL GROUP via N-CARBOXYLATE ION EQUIVALENT

Sakaitani, Masahiro,Ohfune, Yasufumi

, p. 5543 - 5546 (2007/10/02)

Reaction of a variety of N-t-butoxycarbonyl compounds with t-butyldimethylsilyl trifluoromethanesulfonate afforded the N-t-butyldimethylsilyloxycarbonyl compounds, chemoselectively, which upon treatment with an alkyl or aryl halide provided the corresponding N-alkoxy- or N-aryloxycarbonyl compounds, efficiently.

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