602-10-8

Basic information

• Product Name: 1-Nitro-2-anthraquinonecarbonyl chloride
• Synonyms: 1-Nitro-2-anthraquinonecarbonyl chloride;1-nitro-9,10-dioxo-anthracene-2-carbonyl chloride;1-nitro-9,10-dioxoanthracene-2-carbonyl chloride;9,10-diketo-1-nitro-anthracene-2-carbonyl chloride
• CAS NO: 602-10-8
• Molecular Formula: C₁₅H₆ClNO₅
• Molecular Weight: 315.66484
• Mol File: 602-10-8.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 543.2°C at 760 mmHg
• Flash Point: 282.3°C
• Appearance: /
• Density: 1.599g/cm³
• Vapor Pressure: 7.36E-12mmHg at 25°C
• Refractive Index: 1.69
• CAS DataBase Reference: 1-Nitro-2-anthraquinonecarbonyl chloride(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Nitro-2-anthraquinonecarbonyl chloride(602-10-8)
• EPA Substance Registry System: 1-Nitro-2-anthraquinonecarbonyl chloride(602-10-8)

Safety Data

• Hazardous Substances Data: 602-10-8(Hazardous Substances Data)

Usage

General Description

1-Nitro-2-anthraquinonecarbonyl chloride is a chemical compound with the molecular formula C15H7ClNO5. It is a yellow crystalline solid that is commonly used as a precursor in the synthesis of various organic compounds. 1-Nitro-2-anthraquinonecarbonyl chloride is known for its reactivity as a carbonyl chloride, making it a versatile building block in organic chemistry. It is commonly utilized in the production of dyes, pigments, and pharmaceuticals, due to its ability to undergo various chemical reactions and form complex molecular structures. 1-Nitro-2-anthraquinonecarbonyl chloride is known for its strong odor and should be handled with care due to its irritant properties.

InChI:InChI=1/C15H6ClNO5/c16-15(20)10-6-5-9-11(12(10)17(21)22)14(19)8-4-2-1-3-7(8)13(9)18/h1-6H

Upstream product

• 129-15-7 1-nitro-2-methylanthraquinone 
• 84-54-8 2-methylanthracene-9,10-dione 
• 128-67-6 1-nitroanthraquinone-2-carboxylic acid 

Downstream Products

• 89972-33-8 1-Nitro-9,10-dioxo-9,10-dihydro-anthracene-2-carboxylic acid (3-methoxy-phenyl)-amide 
• 52740-90-6 1-amino-9,10-dioxo-9,10-dihydro-anthracene-2-carboxylic acid-(3-bromo-9,10-dioxo-9,10-dihydro-[2]anthrylamide) 
• 111413-43-5 6-oxo-2,6-dihydro-dibenz[cd,g]indazole-3-carboxylic acid anilide 
• 89972-23-6 1-H-2-phenylanthra<1,2-d>pyrazoline-3,6,11-trione 
• 430433-69-5 N-benzyl-1-ethylthio-9,10-dioxo-9,10-dihydroanthracene-2-carboxamide 
• 610788-23-3 2-benzyl-2,3,6,11-tetrahydroanthra[2,1-d]isothiazole-3,6,11-trione 
• 430433-66-2 N-benzyl-1-methylthio-9,10-dioxo-9,10-dihydroanthracene-2-carboxamide 
• 430433-68-4 1-ethylthio-9,10-dioxo-9,10-dihydroanthracene-2-carboxanilide 
• 430433-65-1 1-methylthio-9,10-dioxo-9,10-dihydroanthracene-2-carboxanilide 
• 442631-97-2 2-phenyl-2,3,6,11-tetrahydroanthra[2,1-d]isothiazole-3,6,11-trione 
• 100440-95-7 1-Azido-9,10-dioxo-9,10-dihydro-anthracene-2-carboxylic acid (1-phenyl-ethyl)-amide 
• 100440-94-6 1-Azido-9,10-dioxo-9,10-dihydro-anthracene-2-carboxylic acid benzylamide 
• 100440-93-5 1-Azido-9,10-dioxo-9,10-dihydro-anthracene-2-carboxylic acid cyclohexylamide 
• 100440-80-0 6-Oxo-6H-anthra[1,9-cd]isoxazole-3-carboxylic acid (1-phenyl-ethyl)-amide 

Relevant articles and documents

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Synthesis of linear and angular anthraquinonoisothiazol-3-ones, their S-oxides, and S,S-dioxides

2-Methyltetrahydroanthra[2,3-d]isothiazole-3,5,10-trione and 2-R-tetrahydroanthra[2,1-d]isothiazole-3,6,11-triones were synthesized by the reactions of 3-chloro-9,10-dioxo-9,10-dihydroanthracene-2-carboxamide and 1-nitro-9,10-dioxo-9,10-dihydroanthracene-