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CAS

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1448718-39-5

C12H15NO3 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1448718-39-5 Structure

  • Basic information

    1. Product Name: C12H15NO3
    2. Synonyms: C12H15NO3
    3. CAS NO:1448718-39-5
    4. Molecular Formula:
    5. Molecular Weight: 221.256
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1448718-39-5.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: C12H15NO3(CAS DataBase Reference)
    10. NIST Chemistry Reference: C12H15NO3(1448718-39-5)
    11. EPA Substance Registry System: C12H15NO3(1448718-39-5)

  • 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: 1448718-39-5(Hazardous Substances Data)

1448718-39-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1448718-39-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,8,7,1 and 8 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1448718-39:
(9*1)+(8*4)+(7*4)+(6*8)+(5*7)+(4*1)+(3*8)+(2*3)+(1*9)=195
195 % 10 = 5
So 1448718-39-5 is a valid CAS Registry Number.

1448718-39-5Downstream Products

1448718-39-5Relevant articles and documents

Enantioselective synthesis of anti homoallylic alcohols from terminal alkynes and aldehydes based on concomitant use of a cationic iridium complex and a chiral phosphoric acid

Miura, Tomoya,Nishida, Yui,Morimoto, Masao,Murakami, Masahiro

, p. 11497 - 11500 (2013/09/02)

We report a highly diastereo- and enantioselective synthesis of anti homoallylic alcohols from terminal alkynes via (E)-1-alkenylboronates based upon two catalytic reactions: a cationic iridium complex-catalyzed olefin transposition of (E)-1-alkenylboronates and a chiral phosphoric acid-catalyzed allylation reaction of aldehydes.

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