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1431138-30-5

C14H19N3O2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1431138-30-5 Structure

  • Basic information

    1. Product Name: C14H19N3O2
    2. Synonyms:
    3. CAS NO:1431138-30-5
    4. Molecular Formula:
    5. Molecular Weight: 261.324
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1431138-30-5.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: C14H19N3O2(CAS DataBase Reference)
    10. NIST Chemistry Reference: C14H19N3O2(1431138-30-5)
    11. EPA Substance Registry System: C14H19N3O2(1431138-30-5)

  • 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: 1431138-30-5(Hazardous Substances Data)

1431138-30-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1431138-30-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,3,1,1,3 and 8 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1431138-30:
(9*1)+(8*4)+(7*3)+(6*1)+(5*1)+(4*3)+(3*8)+(2*3)+(1*0)=115
115 % 10 = 5
So 1431138-30-5 is a valid CAS Registry Number.

1431138-30-5Downstream Products

1431138-30-5Relevant articles and documents

Application of radical cation spin density maps toward the prediction of photochemical reactivity between N -methyl-1,2,4-triazoline-3,5-dione and substituted benzenes

Breton, Gary W.,Hoke, Kevin R.

, p. 4697 - 4707 (2013/06/27)

Visible light irradiation of N-methyl-1,2,4-triazoline-3,5-dione in the presence of substituted benzenes is capable of inducing substitution reactions where no reaction takes place thermally. In addition to the formation of 1-arylurazole products resultin

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