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CAS

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1286232-23-2

4-azido-N-(4-nitrophenyl)valeramide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1286232-23-2 Structure

  • Basic information

    1. Product Name: 4-azido-N-(4-nitrophenyl)valeramide
    2. Synonyms: 4-azido-N-(4-nitrophenyl)valeramide
    3. CAS NO:1286232-23-2
    4. Molecular Formula:
    5. Molecular Weight: 263.256
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1286232-23-2.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: 4-azido-N-(4-nitrophenyl)valeramide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-azido-N-(4-nitrophenyl)valeramide(1286232-23-2)
    11. EPA Substance Registry System: 4-azido-N-(4-nitrophenyl)valeramide(1286232-23-2)

  • 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: 1286232-23-2(Hazardous Substances Data)

1286232-23-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1286232-23-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,8,6,2,3 and 2 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1286232-23:
(9*1)+(8*2)+(7*8)+(6*6)+(5*2)+(4*3)+(3*2)+(2*2)+(1*3)=152
152 % 10 = 2
So 1286232-23-2 is a valid CAS Registry Number.

1286232-23-2Relevant articles and documents

New synthetic routes for N-substituted 1,n-diamines. II. Synthesis of selectively N-substituted tetra- and pentamethylenediamines from ω-alkanoic acid derivatives

Ramírez, María A.,Corona, María V.,Ortiz, Gisela,Salerno, Alejandra,Perillo, Isabel A.,Blanco, María M.

, p. 1466 - 1468 (2011/06/10)

A new approach for the synthesis of selectively N-substituted tetra- and pentamethylenediamines 1 (n = 4,5) is described. The method uses N-substituted ω-haloalkanamides 2 as precursors and involves the microwave-promoted conversion into ω-azidocarboxamides 3 and later the reduction of both azido and carboxamide groups with diborane.

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