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methanesulfonic acid 2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-phenyl-propyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

311330-36-6

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311330-36-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 311330-36-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,1,1,3,3 and 0 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 311330-36:
(8*3)+(7*1)+(6*1)+(5*3)+(4*3)+(3*0)+(2*3)+(1*6)=76
76 % 10 = 6
So 311330-36-6 is a valid CAS Registry Number.

311330-36-6Relevant academic research and scientific papers

Fast and Facile Synthesis of 4-Nitrophenyl 2-Azidoethylcarbamate Derivatives from N-Fmoc-Protected α-Amino Acids as Activated Building Blocks for Urea Moiety-Containing Compound Library

Chen, Ying-Ying,Chang, Li-Te,Chen, Hung-Wei,Yang, Chia-Ying,Hsin, Ling-Wei

, p. 131 - 136 (2017/04/24)

A fast and facile synthesis of a series of 4-nitrophenyl 2-azidoethylcarbamate derivatives as activated urea building blocks was developed. The N-Fmoc-protected 2-aminoethyl mesylates derived from various commercially available N-Fmoc-protected α-amino ac

Synthesis and biological evaluation of novel irreversible serine protease inhibitors using amino acid based sulfonyl fluorides as an electrophilic trap

Brouwer, Arwin J.,Ceylan, Tarik,Jonker, Anika M.,Linden, Tima Van Der,Liskamp, Rob M.J.

scheme or table, p. 2397 - 2406 (2011/05/12)

We have designed and synthesized novel irreversible serine protease inhibitors containing aliphatic sulfonyl fluorides as an electrophilic trap. These substituted taurine sulfonyl fluorides derived from taurine or protected amino acids were conveniently s

Synthesis and applications of β-aminoethanesulfonyl azides

Brouwer, Arwin J.,Merkx, Remco,Dabrowska, Katarzyna,Rijkers, Dirk T. S.,Liskamp, Rob M. J.

, p. 455 - 460 (2007/10/03)

A very efficient method for the synthesis of β-aminoethanesulfonyl azides is descibed. These aliphatic sulfonyl azides are accessible starting from a variety of protected amino acids, including those having functionalized side chains. Furthermore, these s

An efficient synthesis of N-protected β-aminoethanesulfonyl chlorides: Versatile building blocks for the synthesis of oligopeptidosulfonamides

Brouwer,Monnee,Liskamp

, p. 1579 - 1584 (2007/10/03)

A very efficient method for the synthesis of β-aminoethanesulfonyl chlorides is described. These aliphatic functionalized sulfonyl chlorides are accessible starting from a variety of protected amino acids, including those having functionalized side chains

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