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14091-31-7

methyl 2-(cyclohexylthio)acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 14091-31-7 Structure

  • Basic information

    1. Product Name: methyl 2-(cyclohexylthio)acetate
    2. Synonyms: methyl 2-(cyclohexylthio)acetate
    3. CAS NO:14091-31-7
    4. Molecular Formula:
    5. Molecular Weight: 188.291
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 14091-31-7.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: methyl 2-(cyclohexylthio)acetate(CAS DataBase Reference)
    10. NIST Chemistry Reference: methyl 2-(cyclohexylthio)acetate(14091-31-7)
    11. EPA Substance Registry System: methyl 2-(cyclohexylthio)acetate(14091-31-7)

  • 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: 14091-31-7(Hazardous Substances Data)

14091-31-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 14091-31-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,0,9 and 1 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 14091-31:
(7*1)+(6*4)+(5*0)+(4*9)+(3*1)+(2*3)+(1*1)=77
77 % 10 = 7
So 14091-31-7 is a valid CAS Registry Number.

14091-31-7Relevant articles and documents

Visible-Light-Mediated Organocatalyzed Thiol-Ene Reaction Initiated by a Proton-Coupled Electron Transfer

Levin, Vitalij V.,Dilman, Alexander D.

, p. 8337 - 8343 (2019/06/27)

A convenient method for performing a thiol-ene reaction is described. The reaction is performed under blue-light irradiation and catalyzed by photoactive Lewis basic molecules such as acridine orange or naphthalene-fused N-acylbenzimidazole. It is believed that the process is initiated by a proton-coupled electron transfer process within the complex between the thiol and the Lewis basic catalyst.

A FACILE ROUTE TO HOMOCHIRAL SULFOXIDES

Burgess, Kevin,Henderson, Ian

, p. 3633 - 3636 (2007/10/02)

Biocatalytic resolution of methyl sulfinylacetates afford sulfoxides (R)-(1)-(6) in very high optical yields; the products have been used in a systematic study of the "SPAC" reaction, an asymmetric synthesis of γ-hydroxy-α,β-unsaturated esters.

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