Details
Stereochemistry | ACHIRAL |
Molecular Formula | C12H12N2.ClH |
Molecular Weight | 220.698 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.NC1=CC=C(NC2=CC=CC=C2)C=C1
InChI
InChIKey=PNEVDCGZQWFIKV-UHFFFAOYSA-N
InChI=1S/C12H12N2.ClH/c13-10-6-8-12(9-7-10)14-11-4-2-1-3-5-11;/h1-9,14H,13H2;1H
Molecular Formula | ClH |
Molecular Weight | 36.461 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Molecular Formula | C12H12N2 |
Molecular Weight | 184.2371 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
Is benzoquinone the prohapten in cross-sensitivity among aminobenzene compounds? | 1998 Dec |
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Contact dermatitis in hairdressers, 10 years later: patch-test results in 300 hairdressers (1994 to 2003) and comparison with previous study. | 2005 Mar |
|
Pi-dimer of an aniline dimer: an ESR-UV-vis spectroelectrochemical study. | 2007 Nov 1 |
|
Role of Mitochondrial Enzymes and Sarcoplasmic ATPase in Cardioprotection Mediated by Aqueous Extract of Desmodium gangeticum (L) DC Root on Ischemic Reperfusion Injury. | 2010 Nov |
|
EPR and ENDOR spectroscopic study of the reactions of aromatic azides with gallium trichloride. | 2010 Nov 21 |
|
p-Anilinoaniline enhancement of dioxin-induced CYP1A1 transcription and aryl hydrocarbon receptor occupancy of CYP1A1 promoter: role of the cell cycle. | 2012 May |
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 17:50:25 GMT 2023
by
admin
on
Fri Dec 15 17:50:25 GMT 2023
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Record UNII |
2TS7135LI6
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Record Status |
Validated (UNII)
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Record Version |
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2TS7135LI6
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218-599-4
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75146
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DTXSID9021132
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Related Record | Type | Details | ||
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PARENT -> SALT/SOLVATE |