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CAS

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913370-08-8

1,2,3-Propanetriol, 1-cyclohexyl-1-phenyl-, (1S,2R)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 913370-08-8 Structure

  • Basic information

    1. Product Name: 1,2,3-Propanetriol, 1-cyclohexyl-1-phenyl-, (1S,2R)-
    2. Synonyms:
    3. CAS NO:913370-08-8
    4. Molecular Formula: C15H22O3
    5. Molecular Weight: 250.338
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 913370-08-8.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: 1,2,3-Propanetriol, 1-cyclohexyl-1-phenyl-, (1S,2R)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,2,3-Propanetriol, 1-cyclohexyl-1-phenyl-, (1S,2R)-(913370-08-8)
    11. EPA Substance Registry System: 1,2,3-Propanetriol, 1-cyclohexyl-1-phenyl-, (1S,2R)-(913370-08-8)

  • 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: 913370-08-8(Hazardous Substances Data)

913370-08-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 913370-08-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,3,3,7 and 0 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 913370-08:
(8*9)+(7*1)+(6*3)+(5*3)+(4*7)+(3*0)+(2*0)+(1*8)=148
148 % 10 = 8
So 913370-08-8 is a valid CAS Registry Number.

913370-08-8Relevant articles and documents

An efficient asymmetric synthesis of (S)-2-cyclohexyl-2-phenylglycolic acid, the acid segment of oxybutynin

Roy, Siddharth,Sharma, Anubha,Chattopadhyay, Nilmadhav,Chattopadhyay, Subrata

, p. 7067 - 7069 (2007/10/03)

An innovative and facile synthesis of the title compound has been developed starting from (R)-cyclohexylidene glyceraldehyde. The key step in the synthesis is a chiral template-driven Grignard addition with absolute diastereocontrol. The other attractive features are the operational simplicity and the use of inexpensive compounds/reagents.

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