74444-81-8

Basic information

• Product Name: 5-Chloro-2-indanone
• Synonyms: 5-Chloro-2-indanone;5-Chloro-1H-inden-2(3H)-one;5-Chloro-indan-2-one;2H-Inden-2-one, 5-chloro-1,3-dihydro-
• CAS NO: 74444-81-8
• Molecular Formula: C₉H₇ClO
• Molecular Weight: 166.60428
• Mol File: 74444-81-8.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 284.2 °C at 760 mmHg
• Flash Point: 127.7 °C
• Appearance: /
• Density: 1.312 g/cm³
• Vapor Pressure: 0.00303mmHg at 25°C
• Refractive Index: 1.6
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 5-Chloro-2-indanone(CAS DataBase Reference)
• NIST Chemistry Reference: 5-Chloro-2-indanone(74444-81-8)
• EPA Substance Registry System: 5-Chloro-2-indanone(74444-81-8)

Safety Data

• Hazardous Substances Data: 74444-81-8(Hazardous Substances Data)

Usage

General Description

5-Chloro-2-indanone is an organic compound that belongs to the class of ketones. It is a white to light yellow solid with the chemical formula C9H7ClO. This chemical is commonly used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. It is also used as a building block in the production of other organic compounds. 5-Chloro-2-indanone is known for its strong odor and should be handled with care due to its potential health hazards. It is important to follow proper safety precautions when handling this chemical, including using protective equipment and working in a well-ventilated area.

InChI:InChI=1/C9H7ClO/c10-8-2-1-6-4-9(11)5-7(6)3-8/h1-3H,4-5H2

Upstream product

• 74444-80-7 Formic acid 5-chloro-1-hydroxy-indan-2-yl ester 
• 3970-52-3 6-chloro-1H-indene 
• 4251-65-4 (4-chlorophenyl)acetaldehyde 
• 104-88-1 4-chlorobenzaldehyde 
• 70090-69-6 1-chloro-4-(prop-2-yn-1-yl)benzene 

Downstream Products

• 73536-83-1 5-chloro-2,3-dihydro-1H-inden-2-ylamine 
• 897365-76-3 (3E/Z)-6-chloro-3-(3-chloro-2-fluorobenzylidene)-1,3-dihydro-2H-indol-2-one 
• 1303609-37-1 (2'R,3S,4'S,5R)-6-chloro-4'-(3-chloro-2-fluorophenyl)-N-(trans-4-hydroxycyclohexyl)-2'-neopentyl-2-oxospiro[indoline-3,3'-pyrrolidine]-5'-carboxamide trifluoroacetate 
• 1303609-36-0 C₄₃H₄₆Cl₂FN₃O₄ 
• 1303609-28-0 C₄₈H₅₈Cl₂FN₃O₄Si 
• 1303609-29-1 MI-519-65-TFA 
• 1303606-44-1 (2′R,3S,4′R,5′R)-6-chloro-4′-(3-chlorophenyl)-N-((1s,3S)-3-hydroxy-3-methylcyclobutyl)-2′-neopentyl-2-oxospiro[indoline-3,3′-pyrrolidine]-5′-carboxamide trifluoroacetic acid 
• 1303609-27-9 C₄₈H₅₈Cl₂FN₃O₄Si 
• 897365-81-0 (3S,3'S,4'R,6'R,8'S,8a'R)-6-chloro-8'-(3-chloro-2-fluorophenyl)-6'-neopentyl-3',4'-diphenyl-3',4',8',8a'-tetrahydrospiro[indoline-3,7'-pyrrolo[2,1-c][1,4]oxazine]-1',2(6'H)-dione 
• 1303607-07-9 (2'R,3S,3'S,5'R)-6-chloro-3'-(3-chloro-2-fluorophenyl)-5'-(2,2-dimethylpropyl)-N-(4-hydroxycyclohexyl)-2-oxospiro[1H-indole-3,4'-pyrrolidine]-2'-carboxamide 
• 74444-76-1 acide amino-2 chloro-5 indane carboxylique-2 

Relevant articles and documents

Biarylphosphonite gold(I) complexes as superior catalysts for oxidative cyclization of propynyl arenes into indan-2-ones

Striking gold: A series of variously functionalized propynyl arenes was smoothly converted into indan-2-ones by a new gold(I)-catalyzed oxidative cyclization process. [LAu]NTf2 (Tf=trifluoromethanesulfonyl) is a superior catalyst both in terms of yield and kinetics for the present transformation. Copyright