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CAS

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117834-83-0

N,N-hexamethylenebenzohydrazide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 117834-83-0 Structure

  • Basic information

    1. Product Name: N,N-hexamethylenebenzohydrazide
    2. Synonyms: N,N-hexamethylenebenzohydrazide
    3. CAS NO:117834-83-0
    4. Molecular Formula:
    5. Molecular Weight: 218.299
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 117834-83-0.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: N,N-hexamethylenebenzohydrazide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N,N-hexamethylenebenzohydrazide(117834-83-0)
    11. EPA Substance Registry System: N,N-hexamethylenebenzohydrazide(117834-83-0)

  • 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: 117834-83-0(Hazardous Substances Data)

117834-83-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 117834-83-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,7,8,3 and 4 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 117834-83:
(8*1)+(7*1)+(6*7)+(5*8)+(4*3)+(3*4)+(2*8)+(1*3)=140
140 % 10 = 0
So 117834-83-0 is a valid CAS Registry Number.

117834-83-0Downstream Products

117834-83-0Relevant articles and documents

Direct Catalytic Symmetrical, Unsymmetrical N,N-Dialkylation and Cyclization of Acylhydrazides Using Alcohols

Thiyagarajan, Subramanian,Gunanathan, Chidambaram

, p. 6617 - 6622 (2020)

Herein, direct N,N-dialkylation of acylhydrazides using alcohols is reported. This catalytic protocol provides one-pot synthesis of both symmetrical and unsymmetrical N,N-disubstituted acylhydrazides using an assortment of primary and secondary alcohols w

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