cas 938-25-0, 1,2-DIAMINONAPHTHALENE | Articles data ｜lookchem

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938-25-0

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A new method for N-N bond cleavage of N,N-disubstituted hydrazines to secondary amines and direct ortho amination of naphthol and its analogues
An unexpected reaction of N,N-disubstituted hydrazine with naphthol and its analogues under simply thermal conditions has been disclosed. 2-Naphthol reacted with various N,N-disubstituted hydrazines under argon to afford 1-amino-2-naphthol and the corresponding secondary amines in excellent yields. Ortho amination of 2-naphthols, hydroxyquinoline, and naphthalenamine occurred when they reacted with N-methyl-N-phenylhydrazine. Copyright
Tang, Qiang,Zhang, Chao,Luo, Meiming
p. 5840 - 5841
(2008/09/19)

Antiproliferative compounds having nitrogen-containing tricyclic ring systems and phenyl substituents
The invention relates to TS-inhibiting compounds of the formula STR1 where W is an alkylene group; D is a structure having two rings that are unsubstituted or substituted, where (i) one ring is a phenyl ring and (ii) the other ring is a phenyl ring or a 6
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(2008/06/13)

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Chemical Properties

Appearance/Colour :brown solid
Melting Point: 92-94°C
Boiling Point: 363.7 °C at 760 mmHg
Flash Point:207.2 °C
Density: 1.234 g/cm³
Solubility:Chloroform (Slightly), DMSO (Slightly)
Storage Temp.:-20°C Freezer, Under Inert Atmosphere
Vapor Pressure: 1.77E-05mmHg at 25°C
Refractive Index: 1.757
PKA: 5.50±0.10(Predicted)
PSA: 52.04000
LogP: 3.16660

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