Cas 124465-67-4,(3aR,4S,6R,7aS)-2-Benzyl-6-(tert-butyl-dimethyl-silanyloxymethyl)-4-ethoxy-hexahydro-pyrano[3,4-c]pyrrol-7-one

124465-67-4

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Basic information

Product Name: (3aR,4S,6R,7aS)-2-Benzyl-6-(tert-butyl-dimethyl-silanyloxymethyl)-4-ethoxy-hexahydro-pyrano[3,4-c]pyrrol-7-one
Synonyms:
CAS NO:124465-67-4
Molecular Formula:
Molecular Weight: 419.637
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: (3aR,4S,6R,7aS)-2-Benzyl-6-(tert-butyl-dimethyl-silanyloxymethyl)-4-ethoxy-hexahydro-pyrano[3,4-c]pyrrol-7-one(CAS DataBase Reference)
NIST Chemistry Reference: (3aR,4S,6R,7aS)-2-Benzyl-6-(tert-butyl-dimethyl-silanyloxymethyl)-4-ethoxy-hexahydro-pyrano[3,4-c]pyrrol-7-one(124465-67-4)
EPA Substance Registry System: (3aR,4S,6R,7aS)-2-Benzyl-6-(tert-butyl-dimethyl-silanyloxymethyl)-4-ethoxy-hexahydro-pyrano[3,4-c]pyrrol-7-one(124465-67-4)

Safety Data

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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 124465-67-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 124465-67-4 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 7 respectively.
Calculate Digit Verification of CAS Registry Number 124465-67:
(8*1)+(7*2)+(6*4)+(5*4)+(4*6)+(3*5)+(2*6)+(1*7)=124
124 % 10 = 4
So 124465-67-4 is a valid CAS Registry Number.

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124465-67-4Relevant 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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