Cas 130132-07-9,(R)-4-((S)-3-Allyl-4-methyl-cyclohex-1-enyl)-3-(tert-butyl-dimethyl-silanyloxy)-butyraldehyde

130132-07-9

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Basic information

Product Name: (R)-4-((S)-3-Allyl-4-methyl-cyclohex-1-enyl)-3-(tert-butyl-dimethyl-silanyloxy)-butyraldehyde
Synonyms:
CAS NO:130132-07-9
Molecular Formula:
Molecular Weight: 336.59
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: (R)-4-((S)-3-Allyl-4-methyl-cyclohex-1-enyl)-3-(tert-butyl-dimethyl-silanyloxy)-butyraldehyde(CAS DataBase Reference)
NIST Chemistry Reference: (R)-4-((S)-3-Allyl-4-methyl-cyclohex-1-enyl)-3-(tert-butyl-dimethyl-silanyloxy)-butyraldehyde(130132-07-9)
EPA Substance Registry System: (R)-4-((S)-3-Allyl-4-methyl-cyclohex-1-enyl)-3-(tert-butyl-dimethyl-silanyloxy)-butyraldehyde(130132-07-9)

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: 130132-07-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 130132-07-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,1,3 and 2 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 130132-07:
(8*1)+(7*3)+(6*0)+(5*1)+(4*3)+(3*2)+(2*0)+(1*7)=59
59 % 10 = 9
So 130132-07-9 is a valid CAS Registry Number.

130132-07-9Upstream product

130132-05-7 (R)-4-((S)-3-Allyl-4-methyl-cyclohex-1-enyl)-3-(tert-butyl-dimethyl-silanyloxy)-butyric acid methyl ester

130132-07-9Downstream Products

130132-07-9Relevant academic research and scientific papers

An approach to the synthesis of the hexahydronaphthalene unit of pravastatin

Barrish, Joel C.,Wovkulich, Peter M.,Tang, Peng Cho,Batcho, Andrew D.,Uskokovic, Milan R.

, p. 2235 - 2238 (1990)

The aldehyde 3b is prepared from (S)-pulegone (5) by a series of highly effective transformations, including a stereospecific [2,3]-Wittig rearrangement of the allyl ether of 6, stereoselective selenolactonization of 8c, SN2′ addition to 10 and a stereospecific intramolecular ene reaction of 11b.

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