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CAS

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189130-24-3

(2S)-2-(2-fluoro-biphenyl-4-yl)-propan-1-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 189130-24-3 Structure

  • Basic information

    1. Product Name: (2S)-2-(2-fluoro-biphenyl-4-yl)-propan-1-ol
    2. Synonyms: (2S)-2-(2-fluoro-biphenyl-4-yl)-propan-1-ol
    3. CAS NO:189130-24-3
    4. Molecular Formula:
    5. Molecular Weight: 230.282
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 189130-24-3.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: (2S)-2-(2-fluoro-biphenyl-4-yl)-propan-1-ol(CAS DataBase Reference)
    10. NIST Chemistry Reference: (2S)-2-(2-fluoro-biphenyl-4-yl)-propan-1-ol(189130-24-3)
    11. EPA Substance Registry System: (2S)-2-(2-fluoro-biphenyl-4-yl)-propan-1-ol(189130-24-3)

  • 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: 189130-24-3(Hazardous Substances Data)

189130-24-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 189130-24-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,9,1,3 and 0 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 189130-24:
(8*1)+(7*8)+(6*9)+(5*1)+(4*3)+(3*0)+(2*2)+(1*4)=143
143 % 10 = 3
So 189130-24-3 is a valid CAS Registry Number.

189130-24-3Relevant articles and documents

Chemoenzymatic synthesis of (2S)-2-arylpropanols through a dynamic kinetic resolution of 2-arylpropanals with alcohol dehydrogenases

Galletti, Paola,Emer, Enrico,Gucciardo, Gabriele,Quintavalla, Arianna,Pori, Matteo,Giacomini, Daria

, p. 4117 - 4123 (2010)

We applied Horse Liver Alcohol Dehydrogenase (HLADH) to the enantioselective synthesis of six (2S)-2-arylpropanols, useful intermediates in the synthesis of Profens. The influence of substrate structure and reaction conditions on yields and enantioselectivity were investigated. The high yields and high enantioselectivity towards the (S)-enantiomer obtained in the bioreduction of 2-arylpropionic aldehydes, clearly indicate the achievement of a DKR process through a combination of an enzyme-catalyzed kinetic reduction with a chemical base-catalyzed racemization of the unreacted aldehydes. The racemization step is represented by the keto-enol equilibrium of the aldehyde and can be controlled by modulating pH and reaction conditions.

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