D176605
4,5-Dimethyl-1,2-phenylenediamine
98%
Sinônimo(s):
4,5-Diamino-o-xylene
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About This Item
Fórmula linear:
(CH3)2C6H2(NH2)2
Número CAS:
Peso molecular:
136.19
Número CE:
Número MDL:
Código UNSPSC:
12352100
ID de substância PubChem:
NACRES:
NA.22
Produtos recomendados
Ensaio
98%
forma
powder
pf
127-129 °C (lit.)
temperatura de armazenamento
2-8°C
cadeia de caracteres SMILES
Cc1cc(N)c(N)cc1C
InChI
1S/C8H12N2/c1-5-3-7(9)8(10)4-6(5)2/h3-4H,9-10H2,1-2H3
chave InChI
XSZYBMMYQCYIPC-UHFFFAOYSA-N
Aplicação
Employed in the preparation of transition metal complexes and quinoxalinones.
Código de classe de armazenamento
11 - Combustible Solids
Classe de risco de água (WGK)
WGK 3
Ponto de fulgor (°F)
Not applicable
Ponto de fulgor (°C)
Not applicable
Equipamento de proteção individual
dust mask type N95 (US), Eyeshields, Gloves
Certificados de análise (COA)
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Encontre a documentação dos produtos que você adquiriu recentemente na biblioteca de documentos.
Tijana Bugarcic et al.
Inorganic chemistry, 48(19), 9444-9453 (2009-09-29)
The synthesis and characterization of ruthenium(II) arene complexes of the general formula [(eta(6)-arene)Ru(XY)Z](+), where arene = p-cymene (p-cym), hexamethylbenzene (hmb), or biphenyl (bip), XY = o-phenylenediamine (o-pda), o-benzoquinonediimine (o-bqdi), or 4,5-dimethyl-o-phenylenediamine (dmpda), and Z = Cl, Br, or I, are
M L Karnovsky et al.
Environmental health perspectives, 102 Suppl 10, 43-44 (1994-12-01)
Although great progress has been made in understanding the respiratory burst of leukocytes that produce superoxide (O2-), it is possible that a component or components, might have been overlooked. Furthermore, O2- production and its sequels, though cardinal in bactericidal action
E Mikiciuk-Olasik et al.
Acta poloniae pharmaceutica, 51(3), 231-233 (1994-01-01)
Some of new derivatives of 4-acylquinoxalin-2-one obtained in the reaction of N,N'-bis(chloroacetyl)-4,5-dimethyl-o-phenylenediamine with primary amines are described. Compounds were tested for their anti-HIV activity and as ligands for 99mTc.
M Katayama et al.
Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan, 110(10), 776-782 (1990-10-01)
Twelve purines oxidized with 4,5-dimethyl-o-phenylenediamine (DMPD) was found to react with N-bromosuccinimide (NBS) to give fluorescent derivatives. In this paper, the identification of oxidation and fluorescent products have been described. In compliance with the substituent on purine skelton, three alloxans
Bull. Korean Chem. Soc., 15, 1122-1122 (1994)
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