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(S)-methyl 3-cyclohexyl-3-hydroxy-2,2-dimethylpropanoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 457885-20-0 Structure
  • Basic information

    1. Product Name: (S)-methyl 3-cyclohexyl-3-hydroxy-2,2-dimethylpropanoate
    2. Synonyms:
    3. CAS NO:457885-20-0
    4. Molecular Formula:
    5. Molecular Weight: 214.305
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 457885-20-0.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: (S)-methyl 3-cyclohexyl-3-hydroxy-2,2-dimethylpropanoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: (S)-methyl 3-cyclohexyl-3-hydroxy-2,2-dimethylpropanoate(457885-20-0)
    11. EPA Substance Registry System: (S)-methyl 3-cyclohexyl-3-hydroxy-2,2-dimethylpropanoate(457885-20-0)
  • 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: 457885-20-0(Hazardous Substances Data)

457885-20-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 457885-20-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,5,7,8,8 and 5 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 457885-20:
(8*4)+(7*5)+(6*7)+(5*8)+(4*8)+(3*5)+(2*2)+(1*0)=200
200 % 10 = 0
So 457885-20-0 is a valid CAS Registry Number.

457885-20-0Downstream Products

457885-20-0Relevant articles and documents

Highly enantioselective mukaiyama aldol reactions catalyzed by a chiral oxazaborolidinium ion: Total synthesis of (-)-inthomycin C

Senapati, Bidyut Kumar,Gao, Lizhu,Lee, Sung Il,Hwang, Geum-Sook,Ryu, Do Hyun

supporting information; experimental part, p. 5088 - 5091 (2011/01/05)

A cationic oxazaborolidinium-catalyzed asymmetric Mukaiyama aldol reaction of (1-methoxy-2-methyl-propenyloxy)-trimethylsilane with various aldehydes including α,β-disubstituted acroleins has been developed in high yields and enantioselectivities. The synthetic utility of this methodology was demonstrated in the first short synthesis of naturally occurring inthomycin C in high enantiopurity.

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