Cas 1376712-18-3,(4S,6S,7R,8R,8aS)-6,7-bis(benzyloxy)-4-(4-cyanophenyl)-2,2-dimethyl-6,7,8,8a-tetrahydro-4H-benzo[d][1,3]dioxin-8-yl acetate

1376712-18-3

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Basic information

Product Name: (4S,6S,7R,8R,8aS)-6,7-bis(benzyloxy)-4-(4-cyanophenyl)-2,2-dimethyl-6,7,8,8a-tetrahydro-4H-benzo[d][1,3]dioxin-8-yl acetate
Synonyms: (4S,6S,7R,8R,8aS)-6,7-bis(benzyloxy)-4-(4-cyanophenyl)-2,2-dimethyl-6,7,8,8a-tetrahydro-4H-benzo[d][1,3]dioxin-8-yl acetate
CAS NO:1376712-18-3
Molecular Formula:
Molecular Weight: 539.628
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,6S,7R,8R,8aS)-6,7-bis(benzyloxy)-4-(4-cyanophenyl)-2,2-dimethyl-6,7,8,8a-tetrahydro-4H-benzo[d][1,3]dioxin-8-yl acetate(CAS DataBase Reference)
NIST Chemistry Reference: (4S,6S,7R,8R,8aS)-6,7-bis(benzyloxy)-4-(4-cyanophenyl)-2,2-dimethyl-6,7,8,8a-tetrahydro-4H-benzo[d][1,3]dioxin-8-yl acetate(1376712-18-3)
EPA Substance Registry System: (4S,6S,7R,8R,8aS)-6,7-bis(benzyloxy)-4-(4-cyanophenyl)-2,2-dimethyl-6,7,8,8a-tetrahydro-4H-benzo[d][1,3]dioxin-8-yl acetate(1376712-18-3)

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: 1376712-18-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1376712-18-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,6,7,1 and 2 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1376712-18:
(9*1)+(8*3)+(7*7)+(6*6)+(5*7)+(4*1)+(3*2)+(2*1)+(1*8)=173
173 % 10 = 3
So 1376712-18-3 is a valid CAS Registry Number.

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1376712-18-3Relevant academic research and scientific papers

Highly diastereoselective Morita-Baylis-Hillman chemistry: A remote activation effect in the diastereoface selective synthesis of densely functionalized branched cyclic enones from d-glucose

Kumar, Vikas,Ghosal, Partha,Das, Pintu,Shaw, Arun K.

, p. 449 - 456 (2012/07/28)

A highly diastereoselective C-2 alkylation of sugar derived cyclic enone 1 in the presence of diethylaluminium iodide by utilizing Morita-Baylis-Hillman chemistry is reported. While diethylaluminium iodide was found to be a suitable Lewis acid for this tr

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