| Weight | 327.727 g/mol |
|---|---|
| Formula | C16H10ClN3O3 |
| Hydrogen Acceptors | 5 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 3 |
Pigment red 4 (2814-77-9)
1-((2-chloro-4-nitrophenyl)azo)-2-naphthol · D.C. Red No. 36
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- Formation of red pigment by a two-step 2-thiobarbituric acid reaction of alka-2,4-dienals. Potential products of lipid oxidation (Lipids, 1988)
- 1,4-Benzothiazines as Key Intermediates in the Biosynthesis of Red Hair Pigment Pheomelanins (Pigment Cell Research, 2003)
- Thermodynamic and kinetic properties of a red wine pigment: catechin-(4,8)-malvidin-3-O-glucoside. (Journal of Physical Chemistry B, 2010)
- Chemical characterization of a red pigment (5,8-dihydroxy-2,7-dimethoxy-1,4-naphthalenedione) produced by Arthrographis cuboidea in pink stained wood (Holzforschung, 1995)
- The crystal structure of a third polymorph () of C.I. Pigment Red 1, 1-[(4-nitrophenyl)azo]-2-naphthol (Zeitschrift Fur Kristallographie, 1980)
- Preferential interactions in pigmented, polymer blends C.I. Pigment Blue 15:4 and C.I. Pigment Red 122 as used in a poly(carbonate)poly(butylene terephthalate) polymer blend (Journal of Chromatography A, 2005)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 1-((2-chloro-4-nitrophenyl)azo)-2-naphthol
- D.C. Red No. 36
-
SMILESC1=CC=C2C(=C1)C=CC(=O)C2=NNC3=C(C=C(C=C3)[N+](=O)[O-])Cl
-
InChIKeyWJJZURXPOSMHKT-UHFFFAOYSA-N
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