Cas 867344-52-3,(2S,3S)-3-Methyl-1-trityl-aziridine-2-carboxylic acid [((S)-1-benzylcarbamoyl-2-phenyl-ethylcarbamoyl)-methyl]-amide

867344-52-3

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Basic information

Product Name: (2S,3S)-3-Methyl-1-trityl-aziridine-2-carboxylic acid [((S)-1-benzylcarbamoyl-2-phenyl-ethylcarbamoyl)-methyl]-amide
Synonyms: (2S,3S)-3-Methyl-1-trityl-aziridine-2-carboxylic acid [((S)-1-benzylcarbamoyl-2-phenyl-ethylcarbamoyl)-methyl]-amide
CAS NO:867344-52-3
Molecular Formula:
Molecular Weight: 636.794
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: (2S,3S)-3-Methyl-1-trityl-aziridine-2-carboxylic acid [((S)-1-benzylcarbamoyl-2-phenyl-ethylcarbamoyl)-methyl]-amide(CAS DataBase Reference)
NIST Chemistry Reference: (2S,3S)-3-Methyl-1-trityl-aziridine-2-carboxylic acid [((S)-1-benzylcarbamoyl-2-phenyl-ethylcarbamoyl)-methyl]-amide(867344-52-3)
EPA Substance Registry System: (2S,3S)-3-Methyl-1-trityl-aziridine-2-carboxylic acid [((S)-1-benzylcarbamoyl-2-phenyl-ethylcarbamoyl)-methyl]-amide(867344-52-3)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 867344-52-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 867344-52-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,7,3,4 and 4 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 867344-52:
(8*8)+(7*6)+(6*7)+(5*3)+(4*4)+(3*4)+(2*5)+(1*2)=203
203 % 10 = 3
So 867344-52-3 is a valid CAS Registry Number.

867344-52-3Upstream product

867344-52-3Downstream Products

867344-52-3Relevant academic research and scientific papers

Conjugation of selenols with aziridine-2-carboxylic acid-containing peptides

Ide, Nathan D.,Galoni?, Danica P.,Van Der Donk, Wilfred A.,Gin, David Y.

, p. 2011 - 2014 (2007/10/03)

The addition of PhSeH to aziridine-2-carboxylic acid containing peptides is described, thus expanding the scope of nucleophiles for the opening of this class of electrophilic peptide substrates. The process offers a new strategy for the generation of usef

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