Cas 1316220-73-1,(2S,3S)-ethyl N-[tert-butyl-(S)-sulfinyl]-3-methyl-3-phenylaziridine-2-carboxylate

1316220-73-1

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Basic information

Product Name: (2S,3S)-ethyl N-[tert-butyl-(S)-sulfinyl]-3-methyl-3-phenylaziridine-2-carboxylate
Synonyms: (2S,3S)-ethyl N-[tert-butyl-(S)-sulfinyl]-3-methyl-3-phenylaziridine-2-carboxylate
CAS NO:1316220-73-1
Molecular Formula:
Molecular Weight: 309.43
EINECS: N/A
Product Categories: N/A
Mol File: 1316220-73-1.mol
Article Data: 1

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)-ethyl N-[tert-butyl-(S)-sulfinyl]-3-methyl-3-phenylaziridine-2-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: (2S,3S)-ethyl N-[tert-butyl-(S)-sulfinyl]-3-methyl-3-phenylaziridine-2-carboxylate(1316220-73-1)
EPA Substance Registry System: (2S,3S)-ethyl N-[tert-butyl-(S)-sulfinyl]-3-methyl-3-phenylaziridine-2-carboxylate(1316220-73-1)

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: 1316220-73-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1316220-73-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,6,2,2 and 0 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1316220-73:
(9*1)+(8*3)+(7*1)+(6*6)+(5*2)+(4*2)+(3*0)+(2*7)+(1*3)=111
111 % 10 = 1
So 1316220-73-1 is a valid CAS Registry Number.

1316220-73-1Upstream product

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1316220-73-1Relevant articles and documents

Stereoselective aza-Darzens reactions of tert-butanesulfinimines: Convenient access to chiral aziridines

Sola, Toni Moragas,Churcher, Ian,Lewis, William,Stockman, Robert A.

supporting information; experimental part, p. 5034 - 5035 (2011/08/22)

Stereoselective synthesis of 2,3-di- and 2,2′,3-tri-substituted aziridines in good yields and excellent diastereoselectivities are achieved through aza-Darzens reactions of a range of tert-butanesulfinyl aldimines and ketimines with ethyl bromoacetate. Th

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