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CAS

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1262053-50-8

4-(4-bromo-(13)C6-phenyl)-4-oxobutanoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1262053-50-8 Structure

  • Basic information

    1. Product Name: 4-(4-bromo-(13)C6-phenyl)-4-oxobutanoic acid
    2. Synonyms: 4-(4-bromo-(13)C6-phenyl)-4-oxobutanoic acid
    3. CAS NO:1262053-50-8
    4. Molecular Formula:
    5. Molecular Weight: 263.018
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1262053-50-8.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: 4-(4-bromo-(13)C6-phenyl)-4-oxobutanoic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-(4-bromo-(13)C6-phenyl)-4-oxobutanoic acid(1262053-50-8)
    11. EPA Substance Registry System: 4-(4-bromo-(13)C6-phenyl)-4-oxobutanoic acid(1262053-50-8)

  • 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: 1262053-50-8(Hazardous Substances Data)

1262053-50-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1262053-50-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,2,0,5 and 3 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1262053-50:
(9*1)+(8*2)+(7*6)+(6*2)+(5*0)+(4*5)+(3*3)+(2*5)+(1*0)=118
118 % 10 = 8
So 1262053-50-8 is a valid CAS Registry Number.

1262053-50-8Relevant articles and documents

A method for the preparation of [13C6]-labelled 2-substituted naphthalenes

Ellames, George J.,Herbert, John M.

, p. 801 - 803 (2010)

A reliable route is described for the preparation of various 2-substituted derivatives of [1,2,3,4,4a,8a-13C6]-naphthalene via the bromide 10. The approach is used to prepare [naphthalene-1,2,3,4,4a,8a- 13C6]-2-

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