Cas 93474-61-4,N-((4S,5S,6S)-4,6-Dimethyl-2-oxo-4-vinyl-[1,3]dioxan-5-yl)-benzenesulfonamide

93474-61-4

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Basic information

Product Name: N-((4S,5S,6S)-4,6-Dimethyl-2-oxo-4-vinyl-[1,3]dioxan-5-yl)-benzenesulfonamide
Synonyms: N-((4S,5S,6S)-4,6-Dimethyl-2-oxo-4-vinyl-[1,3]dioxan-5-yl)-benzenesulfonamide
CAS NO:93474-61-4
Molecular Formula:
Molecular Weight: 311.359
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: N-((4S,5S,6S)-4,6-Dimethyl-2-oxo-4-vinyl-[1,3]dioxan-5-yl)-benzenesulfonamide(CAS DataBase Reference)
NIST Chemistry Reference: N-((4S,5S,6S)-4,6-Dimethyl-2-oxo-4-vinyl-[1,3]dioxan-5-yl)-benzenesulfonamide(93474-61-4)
EPA Substance Registry System: N-((4S,5S,6S)-4,6-Dimethyl-2-oxo-4-vinyl-[1,3]dioxan-5-yl)-benzenesulfonamide(93474-61-4)

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: 93474-61-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 93474-61-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,4,7 and 4 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 93474-61:
(7*9)+(6*3)+(5*4)+(4*7)+(3*4)+(2*6)+(1*1)=154
154 % 10 = 4
So 93474-61-4 is a valid CAS Registry Number.

93474-61-4Upstream product

93474-61-4Downstream Products

93474-61-4Relevant academic research and scientific papers

α-Amino Acids as Chiral Educts for Asymmetric Products. Chirospecific Syntheses of Methyl L-Sibirosaminide and Its C-3 Epimer from L-Allothreonine

Maurer, Peter J.,Knudsen, Christopher G.,Palkowitz, Alan D.,Papoport, Henry

, p. 325 - 332 (2007/10/02)

Efficient syntheses of methyl L-sibirosaminide and its C-3 epimer are described using L-allothreonine as the chiral educt.Amino acylations of organometallics with the lithium salt of N-(phenylsulfonyl)-L-allothreonine constitute the key carbon-carbon bond

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