Cas 1161147-22-3,(1R,4S,5R,6R)-4,5,6-tris(benzyloxy)-1-(benzyloxymethyl)cyclohex-2-en-1-yl acetate

1161147-22-3

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Basic information

Product Name: (1R,4S,5R,6R)-4,5,6-tris(benzyloxy)-1-(benzyloxymethyl)cyclohex-2-en-1-yl acetate
Synonyms: (1R,4S,5R,6R)-4,5,6-tris(benzyloxy)-1-(benzyloxymethyl)cyclohex-2-en-1-yl acetate
CAS NO:1161147-22-3
Molecular Formula:
Molecular Weight: 578.705
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: (1R,4S,5R,6R)-4,5,6-tris(benzyloxy)-1-(benzyloxymethyl)cyclohex-2-en-1-yl acetate(CAS DataBase Reference)
NIST Chemistry Reference: (1R,4S,5R,6R)-4,5,6-tris(benzyloxy)-1-(benzyloxymethyl)cyclohex-2-en-1-yl acetate(1161147-22-3)
EPA Substance Registry System: (1R,4S,5R,6R)-4,5,6-tris(benzyloxy)-1-(benzyloxymethyl)cyclohex-2-en-1-yl acetate(1161147-22-3)

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: 1161147-22-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1161147-22-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,6,1,1,4 and 7 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1161147-22:
(9*1)+(8*1)+(7*6)+(6*1)+(5*1)+(4*4)+(3*7)+(2*2)+(1*2)=113
113 % 10 = 3
So 1161147-22-3 is a valid CAS Registry Number.

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1161147-22-3Relevant academic research and scientific papers

Efficient synthesis of (+)-mk7607 and its c-1 epimer via the stereoselective transposition of a tertiary allylic alcohol

Lim, Chaemin,Baek, Dong Jae,Kim, Deukjoon,Youn, So Won,Kim, Sanghee

supporting information; experimental part, p. 2583 - 2586 (2009/10/23)

These studies provide an efficient and stereoselective synthetic route to (+)-MK7607 and its C-1 epimer from a common intermediate in high overall yields. The synthetic methodologies mainly rely on the stereospecific 1,3-allylic transposition of the hinde

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