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(R)-1-cyclohexyl-2-methylpropanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 156569-67-4 Structure
  • Basic information

    1. Product Name: (R)-1-cyclohexyl-2-methylpropanol
    2. Synonyms: (R)-1-cyclohexyl-2-methylpropanol
    3. CAS NO:156569-67-4
    4. Molecular Formula:
    5. Molecular Weight: 156.268
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 156569-67-4.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)-1-cyclohexyl-2-methylpropanol(CAS DataBase Reference)
    10. NIST Chemistry Reference: (R)-1-cyclohexyl-2-methylpropanol(156569-67-4)
    11. EPA Substance Registry System: (R)-1-cyclohexyl-2-methylpropanol(156569-67-4)
  • 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: 156569-67-4(Hazardous Substances Data)

156569-67-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 156569-67-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,6,5,6 and 9 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 156569-67:
(8*1)+(7*5)+(6*6)+(5*5)+(4*6)+(3*9)+(2*6)+(1*7)=174
174 % 10 = 4
So 156569-67-4 is a valid CAS Registry Number.

156569-67-4Downstream Products

156569-67-4Relevant articles and documents

Facile synthesis of chiral isopropyl carbinols with high enantiomeric excess via catalytic enantioselective addition of diisopropylzinc to aldehydes

Yang, Weon Ki,Cho, Byung Tae

, p. 2947 - 2953 (2000)

Highly effective syntheses of chiral alkyl and aryl isopropyl carbinols with high enantiomeric excess (94-98% ee) via catalytic enantioselective addition of diisopropylzinc to aldehydes have been developed.

Enantioselective Hydrogenation of Ketones using Different Metal Complexes with a Chiral PNP Pincer Ligand

Garbe, Marcel,Wei, Zhihong,Tannert, Bianca,Spannenberg, Anke,Jiao, Haijun,Bachmann, Stephan,Scalone, Michelangelo,Junge, Kathrin,Beller, Matthias

supporting information, p. 1913 - 1920 (2019/03/13)

The synthesis of different metal pincer complexes coordinating to the chiral PNP ligand bis(2-((2R,5R)-2,5-dimethyl-phospholanoethyl))amine is described in detail. The characterized complexes with Mn, Fe, Re and Ru as metal centers showed good activities regarding the reduction of several prochiral ketones. Comparing these catalysts, the non-noble metal complexes produced best selectivities not only for aromatic substrates, but also for different kinds of aliphatic ones leading to enantioselectivities up to 99% ee. Theoretical investigations elucidated the mechanism and rationalized the selectivity. (Figure presented.).

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