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Details

Stereochemistry ACHIRAL
Molecular Formula C8H9ClN4
Molecular Weight 196.637
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of (2E)-2-[(4-Chlorophenyl)methylene]hydrazinecarboximidamide

SMILES

NC(=N)N\N=C\C1=CC=C(Cl)C=C1

InChI

InChIKey=UYZKWRHTYCCDMP-LFYBBSHMSA-N
InChI=1S/C8H9ClN4/c9-7-3-1-6(2-4-7)5-12-13-8(10)11/h1-5H,(H4,10,11,13)/b12-5+

HIDE SMILES / InChI

Molecular Formula C8H9ClN4
Molecular Weight 196.637
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 1
Optical Activity NONE

Approval Year

Patents

Patents

Substance Class Chemical
Created
by admin
on Mon Mar 31 19:36:18 GMT 2025
Edited
by admin
on Mon Mar 31 19:36:18 GMT 2025
Record UNII
JD3870DZOE
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NSC-65818
Preferred Name English
(2E)-2-[(4-Chlorophenyl)methylene]hydrazinecarboximidamide
Systematic Name English
DE(2-CHLORO)-4-CHLORO-ICERGUASTAT
Common Name English
Hydrazinecarboximidamide, 2-[(4-chlorophenyl)methylene]-, (2E)-
Systematic Name English
Hydrazinecarboximidamide, 2-[(4-chlorophenyl)methylene]-, (E)-
Systematic Name English
p-chlorobenzylideneaminoguanidine
Common Name English
Hydrazinecarboximidamide, 2-[(4-chlorophenyl)methylene]-
Systematic Name English
Code System Code Type Description
CAS
132685-68-8
Created by admin on Mon Mar 31 19:36:18 GMT 2025 , Edited by admin on Mon Mar 31 19:36:18 GMT 2025
PRIMARY
CAS
13308-88-8
Created by admin on Mon Mar 31 19:36:18 GMT 2025 , Edited by admin on Mon Mar 31 19:36:18 GMT 2025
NON-SPECIFIC STEREOCHEMISTRY
NSC
65818
Created by admin on Mon Mar 31 19:36:18 GMT 2025 , Edited by admin on Mon Mar 31 19:36:18 GMT 2025
PRIMARY
EPA CompTox
DTXSID00879399
Created by admin on Mon Mar 31 19:36:18 GMT 2025 , Edited by admin on Mon Mar 31 19:36:18 GMT 2025
PRIMARY
PUBCHEM
9573442
Created by admin on Mon Mar 31 19:36:18 GMT 2025 , Edited by admin on Mon Mar 31 19:36:18 GMT 2025
PRIMARY
FDA UNII
JD3870DZOE
Created by admin on Mon Mar 31 19:36:18 GMT 2025 , Edited by admin on Mon Mar 31 19:36:18 GMT 2025
PRIMARY
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ACTIVE MOIETY