Cas 1146545-63-2,(4S,5S,6S,1'S)-6-(1'-benzyloxy)ethyl-4-tert-butoxy-1-azabicyclo-[3.2.0]heptan-7-one

1146545-63-2

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Basic information

Product Name: (4S,5S,6S,1'S)-6-(1'-benzyloxy)ethyl-4-tert-butoxy-1-azabicyclo-[3.2.0]heptan-7-one
Synonyms:
CAS NO:1146545-63-2
Molecular Formula:
Molecular Weight: 317.428
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: (4S,5S,6S,1'S)-6-(1'-benzyloxy)ethyl-4-tert-butoxy-1-azabicyclo-[3.2.0]heptan-7-one(CAS DataBase Reference)
NIST Chemistry Reference: (4S,5S,6S,1'S)-6-(1'-benzyloxy)ethyl-4-tert-butoxy-1-azabicyclo-[3.2.0]heptan-7-one(1146545-63-2)
EPA Substance Registry System: (4S,5S,6S,1'S)-6-(1'-benzyloxy)ethyl-4-tert-butoxy-1-azabicyclo-[3.2.0]heptan-7-one(1146545-63-2)

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: 1146545-63-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1146545-63-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,4,6,5,4 and 5 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1146545-63:
(9*1)+(8*1)+(7*4)+(6*6)+(5*5)+(4*4)+(3*5)+(2*6)+(1*3)=152
152 % 10 = 2
So 1146545-63-2 is a valid CAS Registry Number.

1146545-63-2Upstream product

167971-82-6 (4S)-4-tert-butoxy-3,4-dihydro-2H-pyrrole 1-oxide

1146545-63-2Downstream Products

1146545-63-2Relevant academic research and scientific papers

Asymmetric kinugasa reaction of cyclic nitrones and nonracemic acetylenes

Stecko, Sebastian,Mames, Adam,Furman, Bartlomiej,Chmielewski, Marek

experimental part, p. 3094 - 3100 (2009/08/08)

Kinugasa reactions between chiral acetylenes and five-membered nitrones, achiral and bearing a stereogenic center in both enantiomeric forms, proceed in moderate to good yield with high diastereoselectivity affording mostly one dominant product. The first

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