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CAS

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1610010-04-2

C12H13NO2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1610010-04-2 Structure

  • Basic information

    1. Product Name: C12H13NO2
    2. Synonyms: C12H13NO2
    3. CAS NO:1610010-04-2
    4. Molecular Formula:
    5. Molecular Weight: 203.241
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1610010-04-2.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: C12H13NO2(CAS DataBase Reference)
    10. NIST Chemistry Reference: C12H13NO2(1610010-04-2)
    11. EPA Substance Registry System: C12H13NO2(1610010-04-2)

  • 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: 1610010-04-2(Hazardous Substances Data)

1610010-04-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1610010-04-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,1,0,0,1 and 0 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1610010-04:
(9*1)+(8*6)+(7*1)+(6*0)+(5*0)+(4*1)+(3*0)+(2*0)+(1*4)=72
72 % 10 = 2
So 1610010-04-2 is a valid CAS Registry Number.

1610010-04-2Downstream Products

1610010-04-2Relevant articles and documents

Nickel(0)-promoted carboxylation of allenamides with carbon dioxide via a nickelalactone intermediate

Saito, Nozomi,Sugimura, Yasuyuki,Sato, Yoshihiro

supporting information, p. 736 - 740 (2014/04/03)

Nickel(0)-promoted carboxylation of N-allenylamides (allenamides) with carbon dioxide proceeded via a nickelalactone intermediate to give β-amino acid derivatives. It was also found that the regioselectivity at the oxidative addition stage was strongly af

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