Cas 84518-32-1,(2S,3S)-N-t-butoxycarbonyl-3-methyl-2-aziridinecarbonylglycine benzyl ester

84518-32-1

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Basic information

Product Name: (2S,3S)-N-t-butoxycarbonyl-3-methyl-2-aziridinecarbonylglycine benzyl ester
Synonyms: (2S,3S)-N-t-butoxycarbonyl-3-methyl-2-aziridinecarbonylglycine benzyl ester
CAS NO:84518-32-1
Molecular Formula:
Molecular Weight: 348.399
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)-N-t-butoxycarbonyl-3-methyl-2-aziridinecarbonylglycine benzyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (2S,3S)-N-t-butoxycarbonyl-3-methyl-2-aziridinecarbonylglycine benzyl ester(84518-32-1)
EPA Substance Registry System: (2S,3S)-N-t-butoxycarbonyl-3-methyl-2-aziridinecarbonylglycine benzyl ester(84518-32-1)

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: 84518-32-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 84518-32-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,5,1 and 8 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 84518-32:
(7*8)+(6*4)+(5*5)+(4*1)+(3*8)+(2*3)+(1*2)=141
141 % 10 = 1
So 84518-32-1 is a valid CAS Registry Number.

84518-32-1Upstream product

58632-95-4 2-(tert-Butoxycarbonyloxyimino)-2-phenylacetonitrile

84518-32-1Downstream Products

84518-32-1Relevant academic research and scientific papers

Studies on 2-Aziridinecarboxylic Acid. VII. Formation of Dehydroamino Acid Peptides via Isomerization of Peptides Containing 2-Aziridinecarboxylic Acid by Tertiary Amines

Nakajima, Kiichiro,Oda, Hitomi,Okawa, Kenji

, p. 3232 - 3236 (1982)

Peptides containing 1-(α-aminoacyl)-2-aziridinecarboxylic acid were isomerized into the corresponding dehydroamino acid peptides by treatment with the tertiary amines, triethylamine or 1,4-diazabicyclooctane (Dabco).Dehydrohydantoin derivatives wer

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