InChI=1S/C6H8N2/c7-5-3-1-2-4-6(5)8/h1-4H,7-8H2 |
GEYOCULIXLDCMW-UHFFFAOYSA-N |
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hydrogen donor
A molecular entity that can undergo oxidation by the loss of hydrogen atom(s).
Bronsted base
A molecular entity capable of accepting a hydron from a donor (Bronsted acid).
(via organic amino compound )
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View more via ChEBI Ontology
Outgoing
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1,2-phenylenediamine
(CHEBI:34043)
has parent hydride
benzene
(CHEBI:16716)
1,2-phenylenediamine
(CHEBI:34043)
has role
hydrogen donor
(CHEBI:17499)
1,2-phenylenediamine
(CHEBI:34043)
is a
phenylenediamine
(CHEBI:51402)
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Incoming
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4-nitro-1,2-phenylenediamine
(CHEBI:67116)
has functional parent
1,2-phenylenediamine
(CHEBI:34043)
benzimidazole precursor fungicide
(CHEBI:87037)
has functional parent
1,2-phenylenediamine
(CHEBI:34043)
entinostat
(CHEBI:132082)
has functional parent
1,2-phenylenediamine
(CHEBI:34043)
JSH-23
(CHEBI:131326)
has functional parent
1,2-phenylenediamine
(CHEBI:34043)
tacedinaline
(CHEBI:90195)
has functional parent
1,2-phenylenediamine
(CHEBI:34043)
thiophanate
(CHEBI:82060)
has functional parent
1,2-phenylenediamine
(CHEBI:34043)
thiophanate-methyl
(CHEBI:35014)
has functional parent
1,2-phenylenediamine
(CHEBI:34043)
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1,2-Diaminobenzene
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KEGG COMPOUND
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2-Aminoaniline
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ChemIDplus
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2-Phenylene diamine
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KEGG COMPOUND
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o-Phenylenediamine
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KEGG COMPOUND
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OPDA
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ChemIDplus
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phenylene-1,2-dimaine
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ChEBI
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606074
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Reaxys Registry Number
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Reaxys
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95-54-5
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CAS Registry Number
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ChemIDplus
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95-54-5
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CAS Registry Number
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NIST Chemistry WebBook
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23099167
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PubMed citation
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Europe PMC
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23172354
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PubMed citation
|
Europe PMC
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23220522
|
PubMed citation
|
Europe PMC
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23232561
|
PubMed citation
|
Europe PMC
|
23245188
|
PubMed citation
|
Europe PMC
|
23317160
|
PubMed citation
|
Europe PMC
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23323634
|
PubMed citation
|
Europe PMC
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23364618
|
PubMed citation
|
Europe PMC
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23452313
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PubMed citation
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Europe PMC
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2420897
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PubMed citation
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Europe PMC
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9025914
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PubMed citation
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Europe PMC
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