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Hydrazinecarboxylic acid, 4-chlorophenyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 80403-27-6 Structure
  • Basic information

    1. Product Name: Hydrazinecarboxylic acid, 4-chlorophenyl ester
    2. Synonyms:
    3. CAS NO:80403-27-6
    4. Molecular Formula: C7H7ClN2O2
    5. Molecular Weight: 186.598
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 80403-27-6.mol
    9. Article Data: 2
  • 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: Hydrazinecarboxylic acid, 4-chlorophenyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: Hydrazinecarboxylic acid, 4-chlorophenyl ester(80403-27-6)
    11. EPA Substance Registry System: Hydrazinecarboxylic acid, 4-chlorophenyl ester(80403-27-6)
  • 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: 80403-27-6(Hazardous Substances Data)

80403-27-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 80403-27-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,4,0 and 3 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 80403-27:
(7*8)+(6*0)+(5*4)+(4*0)+(3*3)+(2*2)+(1*7)=96
96 % 10 = 6
So 80403-27-6 is a valid CAS Registry Number.

80403-27-6Relevant articles and documents

Ortho substituent effects on transfer of aryl groups from oxygen to carbon in adducts from diaryloxycarbenes and DMAD

Lu, Xiaosong,Warkentin, John

, p. 228 - 234 (2007/10/03)

Diaryloxycarbenes, generated by thermolysis of 2,2-diaryloxy-5,5-dimethyl-Δ3-1,3,4-oxadiazolines in benzene, reacted with dimethyl acetylenedicarboxylate (DMAD) to afford triesters. The triesters arose by aryl-group transfer from oxygen to carb

Synthesis of ring-substituted phenyl hydrazinecarboxylates and study of their protonation in dimethyl sulfoxide solutions

Vlasak, Petr,Parik, Patrik,Klicnar, Jiri,Mindl, Jaromir

, p. 793 - 802 (2007/10/03)

The pKa values of nineteen phenyl hydrazinecarboxylate hydrochlorides R-C6H4OCONHNH2.HCl (R = H, 3-and 4-Cl, 3-and 4-O2N, 4-Me) and their 1-methyl or 2-methyl derivatives were determined by potentiometric titration with tetrabutylammonium hydroxide in DMSO. IR spectra of the hydrazinecarboxylates and their hydrochlorides revealed that the hydrazinecarboxylate protonation occurs at N2. The methods of synthesis of phenyl hydrazinecarboxylate and their N-methyl derivatives were optimized.

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