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6-Chloro-1-tetralone

6-Chloro-1-tetralone Suppliers list
Company Name: Zhengzhou TRIZ Pharmaceutical Technology Co., Ltd.  Gold
Tel: 19943855286
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Company Name: Changzhou Kechem Bio-Scientific Co., LTD.  Gold
Tel: 0519-68985668 13685222090
Email: sales@kechem.cn
Company Name: Wuhan EnTai Technology Development Co,.Ltd  
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Company Name: TCI (Shanghai) Development Co., Ltd.  
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Company Name: Energy Chemical  
Tel: 400-0056266
Email: sales8178@energy-chemical.com

6-Chloro-1-tetralone manufacturers

  • 6-Chloro-1-tetralone
  • 6-Chloro-1-tetralone pictures
  • 2026-10-29
  • CAS:26673-31-4
  • Min. Order: 1KG
  • Purity: 98%min
  • Supply Ability: 30tons/month
  • 5-chloro-l-indomone
  • 5-chloro-l-indomone pictures
  • $200.00
  • 2026-09-02
  • CAS:26673-31-4
  • Min. Order: 1KG
  • Purity: 99%, 99.5% Sublimated
6-Chloro-1-tetralone Basic information
Product Name:6-Chloro-1-tetralone
Synonyms:6-CHLORO-TETRAL-1-ON;6-Chloro-1-tetralone;6-Chloro-α-Tetralone;5-CHLORO-L-INDOMONE;6-Chloro-tetral-1-one;6-Chloro-3,4-dihydro-2H-naphthalen-1-one;6-Chloro-1-tetralone 98%;6-chlorotetralin-1-one
CAS:26673-31-4
MF:C10H9ClO
MW:180.63
EINECS:808-038-7
Product Categories:11
Mol File:26673-31-4.mol
6-Chloro-1-tetralone Structure
6-Chloro-1-tetralone Chemical Properties
Melting point 53 °C
Boiling point 150°C/0.7mmHg(lit.)
density 1.248±0.06 g/cm3(Predicted)
refractive index 1.59
storage temp. Keep in dark place,Sealed in dry,Room Temperature
form powder to lump
color White to Yellow to Orange
InChIInChI=1S/C10H9ClO/c11-8-4-5-9-7(6-8)2-1-3-10(9)12/h4-6H,1-3H2
InChIKeyWQKHERPPDYPMNX-UHFFFAOYSA-N
SMILESC1(=O)C2=C(C=C(Cl)C=C2)CCC1
CAS DataBase Reference26673-31-4
Safety Information
WGK Germany WGK 3
HS Code 2914390090
Storage Class11 - Combustible Solids
Hazard ClassificationsAcute Tox. 4 Oral
MSDS Information
6-Chloro-1-tetralone Usage And Synthesis
Uses6-Chloro-1-tetralone is a novel and potent intermediate used for synthesis of pharmaceutical compounds.
SynthesisA solution of sodium nitrite (173 mg, 2.51 mmol) in water (5 mL) at 0 °C (ice-bath) was added to a magnetically stirred suspension of 6-Amino-1-tetralone (360 mg, 2.23 mmol) in aqueous hydrochloric acid (10 mL, 6 M) at 0 °C. This reaction mixture was added dropwise to a solution of copper(I) chloride (267 mg, 2.70 mmol) in concentrated hydrochloric acid (5 mL) at 0 °C. It was allowed to warm up to room 100 temperature and stirred for a further 2 h after which it was neutralised with solid sodium carbonate, extracted with ethyl acetate (3 × 20 mL) and concentrated in vacuo to give slightly yellow oil. This material was subjected to flash chromatography (50% chloroform in hexane) and concentration of the appropriate fractions afforded 6-chloro-1-tetralone (180 mg, 45%) as a waxy solid.
References[1] Patent: US2015/105351, 2015, A1. Location in patent: Paragraph 0440
[2] ACS Medicinal Chemistry Letters, 2014, vol. 5, # 11, p. 1259 - 1262
[3] Organic Letters, 2011, vol. 13, # 24, p. 6488 - 6491
[4] Patent: US2012/302562, 2012, A1. Location in patent: Page/Page column 21
[5] Australian Journal of Chemistry, 2010, vol. 63, # 2, p. 211 - 226
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