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114423-20-0

5-m-Tolyl-pentane-1,2-diol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 114423-20-0 Structure

  • Basic information

    1. Product Name: 5-m-Tolyl-pentane-1,2-diol
    2. Synonyms:
    3. CAS NO:114423-20-0
    4. Molecular Formula:
    5. Molecular Weight: 194.274
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 114423-20-0.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: 5-m-Tolyl-pentane-1,2-diol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5-m-Tolyl-pentane-1,2-diol(114423-20-0)
    11. EPA Substance Registry System: 5-m-Tolyl-pentane-1,2-diol(114423-20-0)

  • 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: 114423-20-0(Hazardous Substances Data)

114423-20-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 114423-20-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,4,2 and 3 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 114423-20:
(8*1)+(7*1)+(6*4)+(5*4)+(4*2)+(3*3)+(2*2)+(1*0)=80
80 % 10 = 0
So 114423-20-0 is a valid CAS Registry Number.

114423-20-0Upstream product

114423-20-0Downstream Products

114423-20-0Relevant articles and documents

Friedel-crafts cyclialkylations of some epoxides. 2. Stereospecificity, substituent, product, and kinetic studies

Taylor, Stephen K.,Davisson, Mark E.,Hissom Jr., B. Rolf,Brown, Sandra L.,Pristach, Holle A.,Schramm, Scott B.,Harvey, Suzanne M.

, p. 425 - 429 (1987)

The relative facility of the cyclialkylation of several arylalkyl epoxides was investigated. Stereochemical studies on the cyclialkylation of cis- and trans-2,3-epoxy-5-phenylpentane establish that the stereospecificity of ring formation is as high as 97%

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