Cas 1585154-00-2,(2E,6E)-9-((S)-3,3-dimethyloxiran-2-yl)-1-(4-methoxy-2,3-dimethylphenyl)-3,7-dimethylnona-2,6-dien-4-yl acetate

1585154-00-2

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Basic information

Product Name: (2E,6E)-9-((S)-3,3-dimethyloxiran-2-yl)-1-(4-methoxy-2,3-dimethylphenyl)-3,7-dimethylnona-2,6-dien-4-yl acetate
Synonyms:
CAS NO:1585154-00-2
Molecular Formula:
Molecular Weight: 414.585
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: (2E,6E)-9-((S)-3,3-dimethyloxiran-2-yl)-1-(4-methoxy-2,3-dimethylphenyl)-3,7-dimethylnona-2,6-dien-4-yl acetate(CAS DataBase Reference)
NIST Chemistry Reference: (2E,6E)-9-((S)-3,3-dimethyloxiran-2-yl)-1-(4-methoxy-2,3-dimethylphenyl)-3,7-dimethylnona-2,6-dien-4-yl acetate(1585154-00-2)
EPA Substance Registry System: (2E,6E)-9-((S)-3,3-dimethyloxiran-2-yl)-1-(4-methoxy-2,3-dimethylphenyl)-3,7-dimethylnona-2,6-dien-4-yl acetate(1585154-00-2)

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: 1585154-00-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1585154-00-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,8,5,1,5 and 4 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1585154-00:
(9*1)+(8*5)+(7*8)+(6*5)+(5*1)+(4*5)+(3*4)+(2*0)+(1*0)=172
172 % 10 = 2
So 1585154-00-2 is a valid CAS Registry Number.

1585154-00-2Upstream product

108-24-7 acetic anhydride

1585154-00-2Downstream Products

1585154-00-2Relevant academic research and scientific papers

Enantioselective total synthesis of (-)-walsucochin B

Xu, Shiyan,Gu, Jixiang,Li, Huilin,Ma, Donghui,Xie, Xingang,She, Xuegong

supporting information, p. 1996 - 1999 (2014/05/06)

The first enantioselective total synthesis of the structurally unique nortriterpenoid (-)-walsucochin B has been accomplished through the cationic polyolefin cyclization initiated by chiral epoxide. The core framework and the stereocenters in the natural

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