Cas 167613-41-4,(2S,3R)-3-(benzyloxy)methyl-2-(tert-butyldimethylsiloxy)methyl-1-<(4-methylphenyl)sulfonyl>aziridine

167613-41-4

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Basic information

Product Name: (2S,3R)-3-(benzyloxy)methyl-2-(tert-butyldimethylsiloxy)methyl-1-<(4-methylphenyl)sulfonyl>aziridine
Synonyms: (2S,3R)-3-(benzyloxy)methyl-2-(tert-butyldimethylsiloxy)methyl-1-<(4-methylphenyl)sulfonyl>aziridine
CAS NO:167613-41-4
Molecular Formula:
Molecular Weight: 461.698
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,3R)-3-(benzyloxy)methyl-2-(tert-butyldimethylsiloxy)methyl-1-<(4-methylphenyl)sulfonyl>aziridine(CAS DataBase Reference)
NIST Chemistry Reference: (2S,3R)-3-(benzyloxy)methyl-2-(tert-butyldimethylsiloxy)methyl-1-<(4-methylphenyl)sulfonyl>aziridine(167613-41-4)
EPA Substance Registry System: (2S,3R)-3-(benzyloxy)methyl-2-(tert-butyldimethylsiloxy)methyl-1-<(4-methylphenyl)sulfonyl>aziridine(167613-41-4)

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: 167613-41-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 167613-41-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,7,6,1 and 3 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 167613-41:
(8*1)+(7*6)+(6*7)+(5*6)+(4*1)+(3*3)+(2*4)+(1*1)=144
144 % 10 = 4
So 167613-41-4 is a valid CAS Registry Number.

167613-41-4Upstream product

167613-41-4Downstream Products

167613-41-4Relevant academic research and scientific papers

Synthesis of optically pure 2-Aziridinemethanols: Versatile synthetic building blocks

Fujii,Nakai,Habashita,Hotta,Tamamura,Otaka,Ibuka

, p. 2241 - 2250 (2007/10/02)

Synthesis of three cis-trans pairs of N-sulfonylated-2-aziridinemethanols starting from (S)-threonine, (R)-allothreonine, a chiral 2-amino alcohol, or enantiomerically enriched 2,3-epoxy alcohols is described. A synthetic route to N-tosyl- and N-mesyl-2-a

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