Cas 135356-72-8,(1R,3R,4S,8S,9R)-(+)-3-carbomethoxy-4,6,10,10-tetramethyltricyclo<7.1.1.0<sup>3,8</sup>>undec-5-en-2-one

135356-72-8

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Basic information

Product Name: (1R,3R,4S,8S,9R)-(+)-3-carbomethoxy-4,6,10,10-tetramethyltricyclo<7.1.1.0^3,8>undec-5-en-2-one
Synonyms: (1R,3R,4S,8S,9R)-(+)-3-carbomethoxy-4,6,10,10-tetramethyltricyclo<7.1.1.0^3,8>undec-5-en-2-one
CAS NO:135356-72-8
Molecular Formula:
Molecular Weight: 276.376
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,4S,8S,9R)-(+)-3-carbomethoxy-4,6,10,10-tetramethyltricyclo<7.1.1.0^3,8>undec-5-en-2-one(CAS DataBase Reference)
NIST Chemistry Reference: (1R,3R,4S,8S,9R)-(+)-3-carbomethoxy-4,6,10,10-tetramethyltricyclo<7.1.1.0^3,8>undec-5-en-2-one(135356-72-8)
EPA Substance Registry System: (1R,3R,4S,8S,9R)-(+)-3-carbomethoxy-4,6,10,10-tetramethyltricyclo<7.1.1.0^3,8>undec-5-en-2-one(135356-72-8)

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: 135356-72-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 135356-72-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,3,5 and 6 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 135356-72:
(8*1)+(7*3)+(6*5)+(5*3)+(4*5)+(3*6)+(2*7)+(1*2)=128
128 % 10 = 8
So 135356-72-8 is a valid CAS Registry Number.

135356-72-8Upstream product

38651-65-9 (1R,5S)-(+)-nopinone

135356-72-8Downstream Products

135356-72-8Relevant academic research and scientific papers

Diels-alder reactions of chiral 5,5-dimethyl-4,6-methano-2-methoxycarbonyl-2-cyclohexenone

Liu, Hsing-Jang,Chew, Sew Yeu,Browne, Eric N.C.

, p. 2005 - 2008 (1991)

Diels-Alder reactions of the chiral enone ester 1 proceed in high yield with addition exclusively to the less hindred Si-face to give adducts of type 5.

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