Cas 1357600-67-9,(3aS,5aR,6R,8aR,1'R,2'E,4'R)-3a,3b,4,5,5a,7,8,8a-octahydro-5a-methyl-6-(1',4',5'-trimethyl-2'-hexenyl)-2H-indeno[5,4-b]furan-2-one

1357600-67-9

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Basic information

Product Name: (3aS,5aR,6R,8aR,1'R,2'E,4'R)-3a,3b,4,5,5a,7,8,8a-octahydro-5a-methyl-6-(1',4',5'-trimethyl-2'-hexenyl)-2H-indeno[5,4-b]furan-2-one
Synonyms: (3aS,5aR,6R,8aR,1'R,2'E,4'R)-3a,3b,4,5,5a,7,8,8a-octahydro-5a-methyl-6-(1',4',5'-trimethyl-2'-hexenyl)-2H-indeno[5,4-b]furan-2-one
CAS NO:1357600-67-9
Molecular Formula:
Molecular Weight: 316.484
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: (3aS,5aR,6R,8aR,1'R,2'E,4'R)-3a,3b,4,5,5a,7,8,8a-octahydro-5a-methyl-6-(1',4',5'-trimethyl-2'-hexenyl)-2H-indeno[5,4-b]furan-2-one(CAS DataBase Reference)
NIST Chemistry Reference: (3aS,5aR,6R,8aR,1'R,2'E,4'R)-3a,3b,4,5,5a,7,8,8a-octahydro-5a-methyl-6-(1',4',5'-trimethyl-2'-hexenyl)-2H-indeno[5,4-b]furan-2-one(1357600-67-9)
EPA Substance Registry System: (3aS,5aR,6R,8aR,1'R,2'E,4'R)-3a,3b,4,5,5a,7,8,8a-octahydro-5a-methyl-6-(1',4',5'-trimethyl-2'-hexenyl)-2H-indeno[5,4-b]furan-2-one(1357600-67-9)

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: 1357600-67-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1357600-67-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,7,6,0 and 0 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1357600-67:
(9*1)+(8*3)+(7*5)+(6*7)+(5*6)+(4*0)+(3*0)+(2*6)+(1*7)=159
159 % 10 = 9
So 1357600-67-9 is a valid CAS Registry Number.

1357600-67-9Upstream product

108-24-7 acetic anhydride

1357600-67-9Downstream Products

1357600-67-9Relevant academic research and scientific papers

Biomimetic Synthesis and Structural Revision of Chaxine B and Its Analogues

Hirata, Yushi,Nakazaki, Atsuo,Kawagishi, Hirokazu,Nishikawa, Toshio

, p. 560 - 563 (2017)

Chaxine B and its analogues were synthesized from ergosterol in eight steps on the basis of our proposed biosynthetic pathway, which includes a highly site-selective and regioselective Baeyer-Villiger oxidation as the key step. This synthesis enabled the revision of the structures of chaxine B and its analogues.

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