Cas 1020068-79-4,[1R,3R,3aS,7R,7aR,1(1R)]-1-(2-benzyloxyhex-5-en-2-yl)-7-isopropyl-3-(2-methylallyl)-hexahydroisobenzofuran-4(1H)-one

1020068-79-4

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Basic information

Product Name: [1R,3R,3aS,7R,7aR,1(1R)]-1-(2-benzyloxyhex-5-en-2-yl)-7-isopropyl-3-(2-methylallyl)-hexahydroisobenzofuran-4(1H)-one
Synonyms: [1R,3R,3aS,7R,7aR,1(1R)]-1-(2-benzyloxyhex-5-en-2-yl)-7-isopropyl-3-(2-methylallyl)-hexahydroisobenzofuran-4(1H)-one
CAS NO:1020068-79-4
Molecular Formula:
Molecular Weight: 424.624
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,3R,3aS,7R,7aR,1(1R)]-1-(2-benzyloxyhex-5-en-2-yl)-7-isopropyl-3-(2-methylallyl)-hexahydroisobenzofuran-4(1H)-one(CAS DataBase Reference)
NIST Chemistry Reference: [1R,3R,3aS,7R,7aR,1(1R)]-1-(2-benzyloxyhex-5-en-2-yl)-7-isopropyl-3-(2-methylallyl)-hexahydroisobenzofuran-4(1H)-one(1020068-79-4)
EPA Substance Registry System: [1R,3R,3aS,7R,7aR,1(1R)]-1-(2-benzyloxyhex-5-en-2-yl)-7-isopropyl-3-(2-methylallyl)-hexahydroisobenzofuran-4(1H)-one(1020068-79-4)

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: 1020068-79-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1020068-79-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,0,0,6 and 8 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1020068-79:
(9*1)+(8*0)+(7*2)+(6*0)+(5*0)+(4*6)+(3*8)+(2*7)+(1*9)=94
94 % 10 = 4
So 1020068-79-4 is a valid CAS Registry Number.

1020068-79-4Upstream product

54340-95-3 1,1-diethoxy-3-methyl-3-butene

1020068-79-4Downstream Products

1020068-81-8 (1R,2S,7R,8R,9R)-9-benzyloxy-6-isopropyl-9,13-dimethyl-15-oxa-tricyclo[6.6.1(1,8).0(2,7)]pentadec-12-en-3-one

1020068-79-4Relevant academic research and scientific papers

Asymmetric total synthesis and X-ray crystal structure of the cytotoxic marine diterpene (+)-vigulariol

Becker, Jochen,Bergander, Klaus,Froehlich, Roland,Hoppe, Dieter

supporting information; experimental part, p. 1654 - 1657 (2009/02/06)

(Figure Presented) A crystal from the China sea: The asymmetric total synthesis of (+)-vigulariol (see picture: red O, blue C, white H) has been accomplished in eight linear steps starting from (R)-cryptone, which is readily available from eucalyptus oil. Key steps involve an asymmetric homoaldol reaction of chiral allyl carbamates and THF cyclocondensation. Ring-closing metathesis led to the tricyclic framework of the cladiellin diterpenes.

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