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1402042-32-3

C21H24N3O(1+)*Cl(1-) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1402042-32-3 Structure

  • Basic information

    1. Product Name: C21H24N3O(1+)*Cl(1-)
    2. Synonyms: C21H24N3O(1+)*Cl(1-)
    3. CAS NO:1402042-32-3
    4. Molecular Formula:
    5. Molecular Weight: 369.894
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1402042-32-3.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: C21H24N3O(1+)*Cl(1-)(CAS DataBase Reference)
    10. NIST Chemistry Reference: C21H24N3O(1+)*Cl(1-)(1402042-32-3)
    11. EPA Substance Registry System: C21H24N3O(1+)*Cl(1-)(1402042-32-3)

  • 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: 1402042-32-3(Hazardous Substances Data)

1402042-32-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1402042-32-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,0,2,0,4 and 2 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1402042-32:
(9*1)+(8*4)+(7*0)+(6*2)+(5*0)+(4*4)+(3*2)+(2*3)+(1*2)=83
83 % 10 = 3
So 1402042-32-3 is a valid CAS Registry Number.

1402042-32-3Downstream Products

1402042-32-3Relevant articles and documents

Pd(0)-catalyzed decarboxylative coupling and tandem C-H arylation/decarboxylation for the synthesis of heteroaromatic biaryls

Nandi, Debkumar,Jhou, Yang-Ming,Lee, Jhen-Yi,Kuo, Bing-Chiuan,Liu, Chien-Yu,Huang, Pei-Wen,Lee, Hon Man

, p. 9384 - 9390 (2012)

An effective Pd(0) carbene complex was successfully employed in the decarboxylative coupling of the heteroaromatic carboxylic acids (imidazo[1,2-a]pyridine and isoxazole) with aryl halides. For carboxyindoles, either decarboxylative coupling or tandem C-H arylation and decarboxylation occurred, leading to the formation of C2-monoarylated indoles.

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