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1373126-09-0

C12H12O2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1373126-09-0 Structure

  • Basic information

    1. Product Name: C12H12O2
    2. Synonyms:
    3. CAS NO:1373126-09-0
    4. Molecular Formula:
    5. Molecular Weight: 188.226
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1373126-09-0.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: C12H12O2(CAS DataBase Reference)
    10. NIST Chemistry Reference: C12H12O2(1373126-09-0)
    11. EPA Substance Registry System: C12H12O2(1373126-09-0)

  • 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: 1373126-09-0(Hazardous Substances Data)

1373126-09-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1373126-09-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,3,1,2 and 6 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1373126-09:
(9*1)+(8*3)+(7*7)+(6*3)+(5*1)+(4*2)+(3*6)+(2*0)+(1*9)=140
140 % 10 = 0
So 1373126-09-0 is a valid CAS Registry Number.

1373126-09-0Upstream product

1373126-09-0Downstream Products

1373126-09-0Relevant articles and documents

Modular synthesis of optically active lactones by Ru-catalyzed asymmetric allylic carboxylation and ring-closing metathesis reaction

Takii, Koichiro,Kanbayashi, Naoya,Onitsuka, Kiyotaka

, p. 3872 - 3874 (2012)

A new synthetic route to optically active unsaturated γ- and δ-lactones has been demonstrated via asymmetric allylic carboxylation with a planar-chiral Cp′Ru catalyst and ring-closing metathesis reaction with a Grubbs II catalyst, and successfully applied to the enantioselective synthesis of (R)-(-)-massoialactone. The Royal Society of Chemistry 2012.

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