7477-59-0

Basic information

• Product Name: 1-chloro-4-methylanthracene-9,10-dione
• Synonyms: 1-Chloro-4-methylanthraquinone; 9,10-Anthracenedione, 1-chloro-4-methyl-; 9,10-Anthracenedione, 9,10-dihydro-1-chloro-4-methyl
• CAS NO: 7477-59-0
• Molecular Formula: C₁₅H₉ClO₂
• Molecular Weight: 256.6838
• Mol File: 7477-59-0.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 437.6°C at 760 mmHg
• Flash Point: 184.6°C
• Density: 1.37g/cm³
• Vapor Pressure: 7.36E-08mmHg at 25°C
• Refractive Index: 1.65
• CAS DataBase Reference: 1-chloro-4-methylanthracene-9,10-dione(CAS DataBase Reference)
• NIST Chemistry Reference: 1-chloro-4-methylanthracene-9,10-dione(7477-59-0)
• EPA Substance Registry System: 1-chloro-4-methylanthracene-9,10-dione(7477-59-0)

Safety Data

• Hazardous Substances Data: 7477-59-0(Hazardous Substances Data)

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

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

Downstream Products

• 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 
• 6268-10-6 4-chloro-9,10-dioxo-9,10-dihydro-1-anthracenecarboxylic acid 
• 15248-05-2 1-Methyl-4-chlor-anthracen 
• 954-07-4 1-methylanthraquinone 
• 610-48-0 1-methylanthracene 
• 4946-86-5 4,4'-bi(1-methylanthraquinone) 
• 4947-19-7 1-anilino-4-methyl-anthraquinone 
• 859332-43-7 1-chloro-4-methyl-9,10-diphenyl-9,10-dihydro-anthracene-9,10-diol 
• 102452-21-1 4-methyl-1-(4'-toluenesulfonamido)-9,10-anthraquinone 
• 866996-78-3 4,4'-dichloro-1,1'-oxalyl-di-anthraquinone 

Relevant articles and documents

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.

EFFECT OF TEMPERATURE, MEDIUM, AND NATURE OF SUBSTITUENTS ON THE THERMAL STAGE IN THE PHOTOCHROMIC TRANSFORMATIONS OF 1-METHYLANTHRAQUINONE DERIVATIVES

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