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CAS

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101514-21-0

1-cyano-1-thiophenyl-3,4-dibenzyloxycyclopentane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 101514-21-0 Structure

  • Basic information

    1. Product Name: 1-cyano-1-thiophenyl-3,4-dibenzyloxycyclopentane
    2. Synonyms:
    3. CAS NO:101514-21-0
    4. Molecular Formula:
    5. Molecular Weight: 415.556
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 101514-21-0.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: 1-cyano-1-thiophenyl-3,4-dibenzyloxycyclopentane(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-cyano-1-thiophenyl-3,4-dibenzyloxycyclopentane(101514-21-0)
    11. EPA Substance Registry System: 1-cyano-1-thiophenyl-3,4-dibenzyloxycyclopentane(101514-21-0)

  • 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: 101514-21-0(Hazardous Substances Data)

101514-21-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 101514-21-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,1,5,1 and 4 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 101514-21:
(8*1)+(7*0)+(6*1)+(5*5)+(4*1)+(3*4)+(2*2)+(1*1)=60
60 % 10 = 0
So 101514-21-0 is a valid CAS Registry Number.

101514-21-0Relevant articles and documents

NOVEL (4+1) FRAGMENT COMBINATION APPROACH TO CHIRAL CYCLOPENTANOIDS FROM TARTARIC ACID

Barriere, Francoise,Barriere, Jean-Claude,Barton, Derek H. R.,Cleophax, Jeanine,Gateau-Olesker, Alice,et al.

, p. 3121 - 3124 (2007/10/02)

A chiral cyclopentanoid building block 29 has been synthesized in a "one pot" cyclization process from epoxides 22-25 (which are readily accessible from (R,R)-(+)-tartaric acid) with the carbanion derived from phenylthioacetonitrile (PhS-CH2-CN).

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