Cas 124465-66-3,(3S,3aR,6aS)-5-Benzyl-3-(tert-butyl-diphenyl-silanyloxymethyl)-hexahydro-furo[3,4-c]pyrrol-1-one

124465-66-3

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Basic information

Product Name: (3S,3aR,6aS)-5-Benzyl-3-(tert-butyl-diphenyl-silanyloxymethyl)-hexahydro-furo[3,4-c]pyrrol-1-one
Synonyms:
CAS NO:124465-66-3
Molecular Formula:
Molecular Weight: 485.698
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: (3S,3aR,6aS)-5-Benzyl-3-(tert-butyl-diphenyl-silanyloxymethyl)-hexahydro-furo[3,4-c]pyrrol-1-one(CAS DataBase Reference)
NIST Chemistry Reference: (3S,3aR,6aS)-5-Benzyl-3-(tert-butyl-diphenyl-silanyloxymethyl)-hexahydro-furo[3,4-c]pyrrol-1-one(124465-66-3)
EPA Substance Registry System: (3S,3aR,6aS)-5-Benzyl-3-(tert-butyl-diphenyl-silanyloxymethyl)-hexahydro-furo[3,4-c]pyrrol-1-one(124465-66-3)

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: 124465-66-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 124465-66-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,4,6 and 5 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 124465-66:
(8*1)+(7*2)+(6*4)+(5*4)+(4*6)+(3*5)+(2*6)+(1*6)=123
123 % 10 = 3
So 124465-66-3 is a valid CAS Registry Number.

124465-66-3Upstream product

124465-66-3Downstream Products

124465-69-6 C₃₅H₃₃NO₆

124465-66-3Relevant academic research and scientific papers

?-Facial Selectivity of the 1,3-Dipolar Cycloaddition of the Parent Azomethine Ylide to Homochiral Dipolarophiles

Wee, Andrew G. H.

, p. 1363 - 1364 (2007/10/02)

The 1,3-dipolar cycloaddition of the azomethine ylide (2) with homochiral cyclic dipolarophiles proceeds with high facial selectivity, whereas for homochiral acyclic dipolarophiles, the ?-facial selectivity and mode of cycloaddition is dependent on the structure of the dipolarophile.

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