7-CHLORO-1-INDANONE

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CAS:34911-25-6
Purity:99% Package:1KG;1USD
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Purity:98% (Min,GC) Package:100g;1kg;5kg,10kg,25kg,50kg
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Purity:97+% Package:1g;10g;100g;;1kg Remarks:Z-06225

7-CHLORO-1-INDANONE manufacturers

  • 7-CHLORO-1-INDANONE
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  • $1.00 / 1KG
  • 2024-08-08
  • CAS:34911-25-6
  • Min. Order: 1KG
  • Purity: 99%
  • Supply Ability: 20T
  • 7-Chloro-1-indanone
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  • $0.00 / 1KG
  • 2022-01-04
  • CAS:34911-25-6
  • Min. Order: 1g
  • Purity: 98%min
  • Supply Ability: 50kgs/month
  • 7-CHLORO-1-INDANONE
  • 7-CHLORO-1-INDANONE pictures
  • $1.00 / 1KG
  • 2019-07-12
  • CAS:34911-25-6
  • Min. Order: 1KG
  • Purity: 99%
  • Supply Ability: 100kg
7-CHLORO-1-INDANONE Basic information
Product Name:7-CHLORO-1-INDANONE
Synonyms:7-CHLORO-1-INDANONE;7-CHLORO-INDAN-1-ONE;7-chloro-2,3-dihydro-1H-inden-1-one;REF DUPL: 7-Chloro-1-indanone;7-chloro-2,3-dihydroinden-1-one;1H-Inden-1-one, 7-chloro-2,3-dihydro-;7-Chlorindan-1-on
CAS:34911-25-6
MF:C9H7ClO
MW:166.6
EINECS:202-110-6
Product Categories:Indane/Indanone and Derivatives
Mol File:34911-25-6.mol
7-CHLORO-1-INDANONE Structure
7-CHLORO-1-INDANONE Chemical Properties
Melting point 98 °C
Boiling point 288.2±29.0 °C(Predicted)
density 1.312±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
AppearanceOff-white to yellow Solid
InChIInChI=1S/C9H7ClO/c10-7-3-1-2-6-4-5-8(11)9(6)7/h1-3H,4-5H2
InChIKeyYNFZQNGHYQYLCF-UHFFFAOYSA-N
SMILESC1(=O)C2=C(C=CC=C2Cl)CC1
CAS DataBase Reference34911-25-6(CAS DataBase Reference)
Safety Information
Hazard Codes Xn
Risk Statements 36/37/38-22
Safety Statements 26-36/37/39
HS Code 2914390090
MSDS Information
7-CHLORO-1-INDANONE Usage And Synthesis
Uses7-Chloro-1-indanone is a reagent used to synthesize tetracyclic quinoline and quinoxaline carboxamides which are used as therapeutic topoisomerase inhibitors.
Synthesis
1-(2-Chlorophenyl)-2-propen-1-one

89638-23-3

7-CHLORO-1-INDANONE

34911-25-6

Dichloromethane (400 mL) was added to the crude product (compound-II-a) under ice bath conditions. A solution of titanium tetrachloride (11.3 g) in dichloromethane (50 mL) was slowly added dropwise, the internal temperature of the reaction system was controlled to be less than 10°C, followed by a slow warming up to room temperature with continuous stirring. The progress of the reaction was monitored by gas chromatography until the amount of raw material remaining was less than 3% (about 8 hours). Upon completion of the reaction, the reaction solution was poured into ice water (~2 L) and extracted with dichloromethane to combine the organic phases. The organic phase was dried over anhydrous sodium sulfate, filtered and concentrated to give the crude product. Purification by fast column chromatography (eluent ratio: ethyl acetate/petroleum ether = 1:10) gave a light yellow solid target product (compound-III-a, 21.66 g) in 65% yield.

References[1] Bioorganic and Medicinal Chemistry, 1999, vol. 7, # 12, p. 2801 - 2809
[2] Patent: CN108164408, 2018, A. Location in patent: Paragraph 0026; 0028; 0030
7-CHLORO-1-INDANONE Preparation Products And Raw materials
Raw materials1-(2-Chlorophenyl)-2-propen-1-one-->Ethylene-->2-Chlorobenzoic acid-->Titanium tetrachloride-->Dichloromethane
Preparation Products7-CHLORO-2,3-DIHYDRO-1H-INDEN-1-OL
Tag:7-CHLORO-1-INDANONE(34911-25-6) Related Product Information
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