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CAS

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205128-02-5

(1R,3R)-3-trifluoromethylcyclohexanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 205128-02-5 Structure

  • Basic information

    1. Product Name: (1R,3R)-3-trifluoromethylcyclohexanol
    2. Synonyms:
    3. CAS NO:205128-02-5
    4. Molecular Formula:
    5. Molecular Weight: 168.159
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 205128-02-5.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: (1R,3R)-3-trifluoromethylcyclohexanol(CAS DataBase Reference)
    10. NIST Chemistry Reference: (1R,3R)-3-trifluoromethylcyclohexanol(205128-02-5)
    11. EPA Substance Registry System: (1R,3R)-3-trifluoromethylcyclohexanol(205128-02-5)

  • 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: 205128-02-5(Hazardous Substances Data)

205128-02-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 205128-02-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,5,1,2 and 8 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 205128-02:
(8*2)+(7*0)+(6*5)+(5*1)+(4*2)+(3*8)+(2*0)+(1*2)=85
85 % 10 = 5
So 205128-02-5 is a valid CAS Registry Number.

205128-02-5Downstream Products

205128-02-5Relevant articles and documents

Trifluoromethyl vs. methyl ability to direct enantioselection in microbial reduction of carbonyl substrates

Arnone, Alberto,Bernardi, Rosanna,Blasco, Francesca,Cardillo, Rosanna,Resnati, Giuseppe,Gerus, Igor I.,Kukhar, Valery P.

, p. 2809 - 2818 (1998)

The stereoselective reduction of 3-trifluoromethylcyclohexanone (1a), (E)-1.1.1-(trifluoro-4-phenyl-3-buten-2-one (3a), and their unfluorinated analogues 1b and 3b has been performed with some growing microorganisms. Differences in the electronic and steric properties of the trifluoromethyl and methyl residues result in different chemo- and stereoselectivities in the microbial reduction of phenylbutenones 3a and 3b while cyclohexanones 1a and 1b showed strictly similar stereoselectivities. A new protocol based oil 13C NMR spectra of 2-phenylpropionic acid esters]has been used to assign the absolute configuration of the obtained secondary alcohols.

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