Weight | 418.496 g/mol |
---|---|
Formula | C28H22N2O2 |
Hydrogen Acceptors | 4 |
Hydrogen Donors | 2 |
Aromatic Rings | 4 |
Rotatable Bonds | 4 |
Solvent green 3 (128-80-3)
1,4-di-4-toluidinoanthraquinone · cyanine green G base · D and C Green #6
Score:
#3198 in Chemistry
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- Copper Nanoparticles on Charcoal for Multicomponent Catalytic Synthesis of 1,2,3Triazole Derivatives from Benzyl Halides or Alkyl Halides, Terminal Alkynes and Sodium Azide in Water as a Green Solvent (Advanced Synthesis & Catalysis, 2009)
- Green chemistry approaches to the synthesis of 5-alkoxycarbonyl-4-aryl-3,4-dihydropyrimidin-2(1H)-ones by a three-component coupling of one-pot condensation reaction: Comparison of ethanol, water, and solvent-free conditions (Journal of Organic Chemistry, 2003)
- Eutectic mixture of choline chloride/urea as a green solvent in synthesis of a coordination polymer: [Zn(O 3 PCH 2 CO 2 )]NH 4 (Inorganic Chemistry Communications, 2005)
- An atom efficient, solvent-free, green synthesis and antimycobacterial evaluation of 2-amino-6-methyl-4-aryl-8-[(E)-arylmethylidene]-5,6,7,8-tetrahydro-4H-pyrano[3,2-c]pyridine-3-carbonitriles (Bioorganic & Medicinal Chemistry Letters, 2007)
- PTSA-catalyzed green synthesis of 1,3,5-triarylbenzene under solvent-free conditions (Green Chemistry, 2010)
- Green one pot solvent-free synthesis of pyrano[2,3-c]-pyrazoles and pyrazolo[1,5-a]pyrimidines. (Molecules, 2010)
-
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 1,4-di-4-toluidinoanthraquinone
- cyanine green G base
- D and C Green #6
- D.C. Green No. 6
-
SMILESCC1=CC=C(C=C1)NC2=C3C(=C(C=C2)NC4=CC=C(C=C4)C)C(=O)C5=CC=CC=C5C3=O
-
InChIKeyTVRGPOFMYCMNRB-UHFFFAOYSA-N
- Pubchem - Solvent green 3
- Wikipedia - D&c green no. 6
Quinizarine Green SS, also called Solvent Green 3, C.I. 61565, Oil Green G, D&C Green #6, is a green dye, an anthraquinone derivative. It has the appearance of a black powder with melting point of 220-221 C.
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