Cas 180515-29-1,(1R,2S,5R)-Menthyl 3-(E)-<2-<(E)-2-<(1R,2S,5R)-menthoxycarbonyl>ethenyl>phenyl>acrylate

180515-29-1

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Basic information

Product Name: (1R,2S,5R)-Menthyl 3-(E)-<2-<(E)-2-<(1R,2S,5R)-menthoxycarbonyl>ethenyl>phenyl>acrylate
Synonyms: (1R,2S,5R)-Menthyl 3-(E)-<2-<(E)-2-<(1R,2S,5R)-menthoxycarbonyl>ethenyl>phenyl>acrylate
CAS NO:180515-29-1
Molecular Formula:
Molecular Weight: 494.715
EINECS: N/A
Product Categories: N/A
Mol File: 180515-29-1.mol
Article Data: 1

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,2S,5R)-Menthyl 3-(E)-<2-<(E)-2-<(1R,2S,5R)-menthoxycarbonyl>ethenyl>phenyl>acrylate(CAS DataBase Reference)
NIST Chemistry Reference: (1R,2S,5R)-Menthyl 3-(E)-<2-<(E)-2-<(1R,2S,5R)-menthoxycarbonyl>ethenyl>phenyl>acrylate(180515-29-1)
EPA Substance Registry System: (1R,2S,5R)-Menthyl 3-(E)-<2-<(E)-2-<(1R,2S,5R)-menthoxycarbonyl>ethenyl>phenyl>acrylate(180515-29-1)

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: 180515-29-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 180515-29-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,0,5,1 and 5 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 180515-29:
(8*1)+(7*8)+(6*0)+(5*5)+(4*1)+(3*5)+(2*2)+(1*9)=121
121 % 10 = 1
So 180515-29-1 is a valid CAS Registry Number.

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180515-29-1Relevant articles and documents

The use of vicinal twofold Heck reaction products in diastereoselective sequential Michael additions - A convenient access to enantiomerically pure six-ring anellated cispentacin derivatives

Voigt, Katharina,Lansky, Annegret,Noltemeyer, Mathias,De Meijere, Armin

, p. 899 - 911 (2007/10/03)

The palladium-catalyzed coupling reactions of various acrylic acid derivatives 2a-e (e.g. methyl, tert-butyl, benzyl, menthyl esters) with 1,2-dibromobenzene (1), 1,2,3-tribromobenzene (4) and 1,2-dibromocyclohexene (6) yielded the correspondingly substit

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