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130132-07-9

(R)-4-((S)-3-Allyl-4-methyl-cyclohex-1-enyl)-3-(tert-butyl-dimethyl-silanyloxy)-butyraldehyde is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 130132-07-9 Structure

  • Basic information

    1. Product Name: (R)-4-((S)-3-Allyl-4-methyl-cyclohex-1-enyl)-3-(tert-butyl-dimethyl-silanyloxy)-butyraldehyde
    2. Synonyms:
    3. CAS NO:130132-07-9
    4. Molecular Formula:
    5. Molecular Weight: 336.59
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 130132-07-9.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: (R)-4-((S)-3-Allyl-4-methyl-cyclohex-1-enyl)-3-(tert-butyl-dimethyl-silanyloxy)-butyraldehyde(CAS DataBase Reference)
    10. NIST Chemistry Reference: (R)-4-((S)-3-Allyl-4-methyl-cyclohex-1-enyl)-3-(tert-butyl-dimethyl-silanyloxy)-butyraldehyde(130132-07-9)
    11. 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

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 130132-07-9(Hazardous Substances Data)

130132-07-9 Usage

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.

130132-07-9Downstream Products

130132-07-9Relevant articles and documents

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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