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860784-76-5

N-(4-PHENOXYPHENYL)-1-HYDRAZINECARBOXAMIDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 860784-76-5 Structure

  • Basic information

    1. Product Name: N-(4-PHENOXYPHENYL)-1-HYDRAZINECARBOXAMIDE
    2. Synonyms: N-(4-PHENOXYPHENYL)-1-HYDRAZINECARBOXAMIDE
    3. CAS NO:860784-76-5
    4. Molecular Formula: C13H13N3O2
    5. Molecular Weight: 243.26
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 860784-76-5.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: N-(4-PHENOXYPHENYL)-1-HYDRAZINECARBOXAMIDE(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-(4-PHENOXYPHENYL)-1-HYDRAZINECARBOXAMIDE(860784-76-5)
    11. EPA Substance Registry System: N-(4-PHENOXYPHENYL)-1-HYDRAZINECARBOXAMIDE(860784-76-5)

  • 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: 860784-76-5(Hazardous Substances Data)

860784-76-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 860784-76-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,0,7,8 and 4 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 860784-76:
(8*8)+(7*6)+(6*0)+(5*7)+(4*8)+(3*4)+(2*7)+(1*6)=205
205 % 10 = 5
So 860784-76-5 is a valid CAS Registry Number.

860784-76-5Downstream Products

860784-76-5Relevant articles and documents

Preparation of substituted semicarbazides from corresponding amines and hydrazines via phenyl carbamates

Hron, Rebecca,Jursic, Branko S.

, p. 1540 - 1543 (2014/03/21)

A simple synthetic procedure for the conversion of amines and hydrazines into substituted semicarbazides was developed. The initial condensation between the desired amine and phenyl chloroformate into phenyl carbamate is followed by the addition of hydrazine under basic conditions. The reaction is tolerable to a variety of functional groups, with mild conditions and high percent yields.

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