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Details

Stereochemistry ACHIRAL
Molecular Formula C12H12N2S
Molecular Weight 216.302
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 4,4'-THIODIANILINE

SMILES

NC1=CC=C(SC2=CC=C(N)C=C2)C=C1

InChI

InChIKey=ICNFHJVPAJKPHW-UHFFFAOYSA-N
InChI=1S/C12H12N2S/c13-9-1-5-11(6-2-9)15-12-7-3-10(14)4-8-12/h1-8H,13-14H2

HIDE SMILES / InChI
4,4'-Thiodianiline is a chemical intermediate that was used in a production of mordant yellow and other dyes. 4,4'-Thiodianiline is reasonably anticipated to be a human carcinogen based on sufficient evidence of carcinogenicity from studies in experimental animals. 4,4'-Thiodianiline has demonstrated anticonvulsant activity in vivo.

CNS Activity

Curator's Comment: Active in rats in the model of epilepsy

Approval Year

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Unknown

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
In vivo evaluation of diaminodiphenyls: anticonvulsant agents with minimal acute neurotoxicity.
2009 Sep 1
Patents

Sample Use Guides

In a model of epilepsy, the compound was administered to rats intraperitoneally at 30 mg/kg
Route of Administration: Intraperitoneal
In Vitro Use Guide
Unknown
Name Type Language
4,4'-THIODIANILINE
HSDB  
Systematic Name English
BENZENAMINE, 4,4'-THIOBIS-
Systematic Name English
4,4'-THIODIANILINE [IARC]
Common Name English
BAPS
Common Name English
4,4'-THIOBISBENZENAMINE
Systematic Name English
BIS(P-AMINOPHENYL) SULFIDE
Common Name English
DI(P-AMINOPHENYL) SULFIDE
Common Name English
NSC-6191
Code English
4,4'-THIODIANILINE [HSDB]
Common Name English
P,P'-DIAMINODIPHENYL SULFIDE
Common Name English
NCI-C01707
Code English
Code System Code Type Description
NCI_THESAURUS
C44322
Created by admin on Fri Dec 15 15:59:21 GMT 2023 , Edited by admin on Fri Dec 15 15:59:21 GMT 2023
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WIKIPEDIA
4,4'-Thiodianiline
Created by admin on Fri Dec 15 15:59:21 GMT 2023 , Edited by admin on Fri Dec 15 15:59:21 GMT 2023
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MESH
C011749
Created by admin on Fri Dec 15 15:59:21 GMT 2023 , Edited by admin on Fri Dec 15 15:59:21 GMT 2023
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EPA CompTox
DTXSID9021344
Created by admin on Fri Dec 15 15:59:21 GMT 2023 , Edited by admin on Fri Dec 15 15:59:21 GMT 2023
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ECHA (EC/EINECS)
205-370-9
Created by admin on Fri Dec 15 15:59:21 GMT 2023 , Edited by admin on Fri Dec 15 15:59:21 GMT 2023
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FDA UNII
6GGU990BQF
Created by admin on Fri Dec 15 15:59:21 GMT 2023 , Edited by admin on Fri Dec 15 15:59:21 GMT 2023
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NSC
6191
Created by admin on Fri Dec 15 15:59:21 GMT 2023 , Edited by admin on Fri Dec 15 15:59:21 GMT 2023
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PUBCHEM
8765
Created by admin on Fri Dec 15 15:59:21 GMT 2023 , Edited by admin on Fri Dec 15 15:59:21 GMT 2023
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CAS
139-65-1
Created by admin on Fri Dec 15 15:59:21 GMT 2023 , Edited by admin on Fri Dec 15 15:59:21 GMT 2023
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HSDB
5074
Created by admin on Fri Dec 15 15:59:21 GMT 2023 , Edited by admin on Fri Dec 15 15:59:21 GMT 2023
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