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5-Bromo-1-indanone

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Company Name: Hebei Chuanghai Biotechnology Co., Ltd
Tel: +8615350571055
Email: Sibel@chuanghaibio.com
Products Intro: Product Name:5-Bromoindanone
CAS:34598-49-7
Purity:99%
Company Name: Henan Fengda Chemical Co., Ltd
Tel: +86-371-86557731 +86-13613820652
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Products Intro: Product Name:5-Bromo-1-indanone
CAS:34598-49-7
Purity:99% Package:1kg;36USD|1000kg;1.5USD
Company Name: Capot Chemical Co.,Ltd.
Tel: +86-(0)57185586718 +86-13336195806
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Products Intro: Product Name:5-Bromo-1-indanone
CAS:34598-49-7
Purity:98% (Min,HPLC) Package:1G;1KG;100KG
Company Name: Henan Tianfu Chemical Co.,Ltd.
Tel: +86-0371-55170693 +86-19937530512
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Products Intro: Product Name:5-Bromoindanone
CAS:34598-49-7
Purity:99% Package:25KG;5KG;1KG
Company Name: career henan chemical co
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Products Intro: Product Name:5-Bromoindanone
CAS:34598-49-7
Purity:99% Package:1KG;100USD

5-Bromo-1-indanone manufacturers

  • 5-Bromoindanone
  • 5-Bromoindanone pictures
  • 2026-03-20
  • CAS:34598-49-7
  • Min. Order: 1KG
  • Purity: 99%
  • Supply Ability: 20 mt
  • 5-Bromoindanone
  • 5-Bromoindanone pictures
  • 2025-04-04
  • CAS:34598-49-7
  • Min. Order: 1KG
  • Purity: 98%
  • Supply Ability: 1Ton
5-Bromo-1-indanone Basic information
Product Name:5-Bromo-1-indanone
Synonyms:5-BROMOINDAN-1-ONE;5-BROMOINDANONE;5-BROMO-1-INDANONE;Anti-AKR1C1 antibody produced in rabbit;17-beta-HSD 2;17-beta-hydroxysteroid dehydrogenase type 2;ANTI-HSD17B2 (CENTER) antibody produced in rabbit;E2DH
CAS:34598-49-7
MF:C9H7BrO
MW:211.06
EINECS:629-357-6
Product Categories:Indane/Indanone and Derivatives;Heterocycles series;Indanone & Indene;Ketone;Fused Ring Systems;Halides;C9;Carbonyl Compounds;Ketones;Carbonyl Compounds;Building Blocks;Chemical Synthesis;Organic Building Blocks
Mol File:34598-49-7.mol
5-Bromo-1-indanone Structure
5-Bromo-1-indanone Chemical Properties
Melting point 126-129 °C(lit.)
Boiling point 303.7±31.0 °C(Predicted)
density 1.18 g/mL at 25 °C(lit.)
refractive index 1.5720 (estimate)
storage temp. Sealed in dry,Room Temperature
form Powder
color Beige to brown
biological sourcerabbit
BRN 2357199
InChIInChI=1S/C9H7BrO/c10-7-2-3-8-6(5-7)1-4-9(8)11/h2-3,5H,1,4H2
InChIKeyKSONICAHAPRCMV-UHFFFAOYSA-N
SMILESC1(=O)C2=C(C=C(Br)C=C2)CC1
CAS DataBase Reference34598-49-7(CAS DataBase Reference)
NIST Chemistry Reference1H-inden-1-one, 5-bromo-2,3-dihydro-(34598-49-7)
Safety Information
Hazard Codes Xn,Xi
Risk Statements 20/21/22-36/37/38-22
Safety Statements 26-36-36/37/39
WGK Germany 3
Hazard Note Harmful
HazardClass IRRITANT
HS Code 29147000
Storage Class11 - Combustible Solids
Hazard ClassificationsAcute Tox. 4 Oral
Eye Irrit. 2
Skin Irrit. 2
STOT SE 3
MSDS Information
ProviderLanguage
SigmaAldrich English
ACROS English
ALFA English
5-Bromo-1-indanone Usage And Synthesis
Description5-Bromo-1-indanone is a 1-indanone derivative. Its physical properties like density, freezing point and refractive index have been determined. It participates in the synthesis of the imidazolyl and triazolyl substituted biphenyl compounds.
Chemical Propertieswhite to light yellow crystal powder
UsesStarter for indanone-based pharmaceuticals1,2
Application5-Bromo-1-indanone is a pharmaceutical intermediate compound that is a raw material for the preparation of indanone-based pharmaceuticals. It is also used as a chemical reagent for the preparation of other indanones such as 2,3,5 tribromoindanone by bromination[1].
General Description5-Bromo-1-indanone is a 1-indanone derivative. Its physical properties like density, freezing point and refractive index have been determined. It participates in the synthesis of the imidazolyl and triazolyl substituted biphenyl compounds.
Synthesis
5-Bromo-2,3-dihydro-1H-inden-1-ol

34598-50-0

5-Bromo-1-indanone

34598-49-7

GENERAL STEPS: Be safe. Tert-butyl hydroperoxide (TBHP) is highly reactive, flammable and toxic, corrosive to skin and mucous membranes, and may cause respiratory distress by inhalation. A solution of 5-bromo-2,3-dihydro-1H-inden-1-ol (1 mmol) with 70% TBHP (6 or 10 equiv.) is reacted with stirring at 100°C for 24 hours. Upon completion of the reaction, the reaction mixture was quenched with saturated sodium thiosulfate solution (5 mL) and subsequently extracted with dichloromethane (3 x 10 mL). The combined dichloromethane extracts were dried with anhydrous Na2SO4, filtered and concentrated under reduced pressure to remove the solvent. The residue was purified by rapid column chromatography on silica gel, and petroleum ether (PE) or mixed solvent of petroleum ether/ethyl acetate (PE/EtOAc) was selected as eluent to finally obtain 5-bromoindanone.

References[1] TUTAR A, YILMAZ M, ERENLER R. Bromination of 4-bromoindanone and 5-bromoindanone[C]. 2013. DOI:10.5151/CHEMPRO-15BMOS-BMOS2013\_20131023104831.
Tag:5-Bromo-1-indanone(34598-49-7) Related Product Information
Pinaverium bromide 5-Methoxy-1-indanone 7-METHOXY-1-INDANONE 97 5-Hydroxy-1-indanone 7-Hydroxy-1-indanone 4-PHENYL-3-BUTYN-2-ONE 1-Indanone Bromine 2-BROMOINDANONE isobromindione 5-BROMO-2-TRIFLUOROACETYL-1-INDANONE 5-BROMO-6-METHOXY-INDAN-1-ONE 6-AMINO-5-BROMO-2,3-DIHYDRO-1H-INDEN-1-ONE 5-Bromo-1-indanone