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133683-67-7

(2RS)-2-<(1R)-3-Cyclohexenyl>-1-propanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 133683-67-7 Structure

  • Basic information

    1. Product Name: (2RS)-2-<(1R)-3-Cyclohexenyl>-1-propanol
    2. Synonyms:
    3. CAS NO:133683-67-7
    4. Molecular Formula:
    5. Molecular Weight: 140.225
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 133683-67-7.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: (2RS)-2-<(1R)-3-Cyclohexenyl>-1-propanol(CAS DataBase Reference)
    10. NIST Chemistry Reference: (2RS)-2-<(1R)-3-Cyclohexenyl>-1-propanol(133683-67-7)
    11. EPA Substance Registry System: (2RS)-2-<(1R)-3-Cyclohexenyl>-1-propanol(133683-67-7)

  • 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: 133683-67-7(Hazardous Substances Data)

133683-67-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 133683-67-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,6,8 and 3 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 133683-67:
(8*1)+(7*3)+(6*3)+(5*6)+(4*8)+(3*3)+(2*6)+(1*7)=137
137 % 10 = 7
So 133683-67-7 is a valid CAS Registry Number.

133683-67-7Downstream Products

133683-67-7Relevant articles and documents

Reductive Carbonylation of Alkenes using Zwitterionic Rhodium Complexes as Catalysts

Zhou, Jian-Qiang,Alper, Howard

, p. 233 - 234 (1991)

Alkenes react with carbon monoxide, sodium borohydride, propan-2-ol and a catalytic amount of Rh(cod)(η6-PhBPh3) (cod = cyclooctadiene) to give alcohols in fine yields; high regioselectivity for the branched or linear alcohol is usually observed, depending on the organic substrate.

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