7477-59-0

Usage

Chemical structure

A derivative of anthracene with a chlorine atom and a methyl group

Physical state

Yellow crystalline solid

Uses

a. Organic synthesis
b. Precursor for dyes and pigments

Potential applications

a. Photocycytotoxic activity
b. Antitumor activity
c. Medical applications (under research)

Toxicity

Low toxicity, no known significant adverse effects to human health or the environment when handled and used appropriately.

Upstream product

• 85-44-9 phthalic anhydride 
• 106-43-4 para-chlorotoluene 
• 73654-13-4 1-Chloro-10-hydroxy-4-methylene-4H-anthracen-9-one 
• 7664-93-9 sulfuric acid 
• 73041-54-0 2-(5'-chloro-2'-methylbenzoyl)benzoic acid 

Downstream Products

• 610-48-0 1-methylanthracene 
• 954-07-4 1-methylanthraquinone 
• 15248-05-2 1-Methyl-4-chlor-anthracen 
• 6268-10-6 4-chloro-9,10-dioxo-9,10-dihydro-1-anthracenecarboxylic acid 
• 866996-78-3 4,4'-dichloro-1,1'-oxalyl-di-anthraquinone 
• 102452-21-1 4-methyl-1-(4'-toluenesulfonamido)-9,10-anthraquinone 
• 4947-19-7 1-anilino-4-methyl-anthraquinone 
• 4946-86-5 4,4'-bi(1-methylanthraquinone) 
• 1403361-81-8 6-(2-benzyloaminoethyloamino)-2,7-dihydro-3H-dibenzo[de,h]cynnolino-3,7-dione 
• 1403361-77-2 2-[2-(piperidinamino)ethyl]-6-(2-benzylaminoethylamino)-2,7-dihydro-3H-dibenzo[de,h]cynnoline-3,7-dione 
• 1403361-57-8 2-[2-(dimethylamino)ethyl]-6-(N-benzylamino)-2,7-dihydro-3H-dibenzo[de,h]cynnoline-3,7-dione 
• 602-69-7 anthraquinone-1-carboxylic acid 
• 607-42-1 anthracene-1-carboxylic acid 
• 859332-43-7 1-chloro-4-methyl-9,10-diphenyl-9,10-dihydro-anthracene-9,10-diol 

Relevant academic research and scientific papers

NOVEL FUSED RING INDAZOLE COMPOUNDS

The present invention provides a novel fused indazole compound having an excellent JNK inhibitory action. More specifically, it provides a compound represented by the following formula, a salt thereof or a hydrate of them. Wherein Z11 and Z12 each independently represent a carbonyl group, a methylene group, etc.;----------- represents a double bond or a single bond; R1a represents a hydrogen atom, etc.; the ring A represents a benzene ring, a naphthalene ring or a 5- to 10-membered aromatic heterocyclic ring, etc.; and R2a, R2b and R2c each independently represent (1) a hydrogen atom, (2) a halogen atom, (3) a nitro group, etc.

THE SYNTHESIS OF SOME MONOMETHYLANTHRACENAMINES

The synthesis of 2-methyl-1-anthracenamine (2), 3-methyl-1-anthracenamine (7), 4-methyl-1-anthracenamine (14), 1-methyl-2-anthracenamine (20), 3-methyl-2-anthracenamine (26), and 1-methyl-3-anthracenamine (3) from the corresponding 9,10-anthraquinones in order to confirm their presence in coal-derived products is reported.

Triazinyl dyes

Vat dyestuffs of the formula EQU1 wherein R represents alkyl with 1 to 4 carbon atoms, R1 and R2 represent hydrogen or alkyl with 1 to 4 carbon atoms and each of A1 and A2 represents a vattable radical with 3 to 7 condensed rings are characterized by improved resistance to alkali and are suitable for dyeing and printing the most diverse materials, in particular fibers made from natural or regenerated cellulose.