CAS 34598-49-7|5-Bromoindanone

Introduction:Basic information about CAS 34598-49-7|5-Bromoindanone, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
Common Name5-Bromoindanone
CAS Number34598-49-7Molecular Weight211.06
Density1.6±0.1 g/cm3Boiling Point303.7±31.0 °C at 760 mmHg
Molecular FormulaC9H7BrOMelting Point126-129 °C(lit.)
MSDSChineseUSAFlash Point120.2±12.2 °C
Symbol
GHS07
Signal WordWarning

Names

Name5-bromo-2,3-dihydroinden-1-one
SynonymMore Synonyms

5-Bromoindanone BiologicalActivity

Description5-Bromo-2,3-dihydro-1H-inden-1-one is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
Related CatalogResearch Areas >>Others

Chemical & Physical Properties

Density1.6±0.1 g/cm3
Boiling Point303.7±31.0 °C at 760 mmHg
Melting Point126-129 °C(lit.)
Molecular FormulaC9H7BrO
Molecular Weight211.06
Flash Point120.2±12.2 °C
Exact Mass209.968018
PSA17.07000
LogP2.86
Vapour Pressure0.0±0.6 mmHg at 25°C
Index of Refraction1.623
Storage condition-20°C

Safety Information

Symbol
GHS07
Signal WordWarning
Hazard StatementsH302-H312-H315-H319-H332-H335
Precautionary StatementsP261-P280-P305 + P351 + P338
Personal Protective Equipmentdust mask type N95 (US);Eyeshields;Gloves
Hazard CodesXn:Harmful
Risk PhrasesR22;R36/37/38
Safety PhrasesS26-S36-S36/37/39
RIDADRNONH for all modes of transport
WGK Germany3
HS Code2914700090

Customs

HS Code2914700090
SummaryHS: 2914700090 halogenated, sulphonated, nitrated or nitrosated derivatives of ketones and quinones, whether or not with other oxygen function Tax rebate rate:9.0% Supervision conditions:none VAT:17.0% MFN tariff:5.5% General tariff:30.0%

Articles8

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Discovery of a series of imidazo[4,5-b]pyridines with dual activity at angiotensin II type 1 receptor and peroxisome proliferator-activated receptor-γ.

J. Med. Chem. 54 , 4219-4233, (2011)

Mining of an in-house collection of angiotensin II type 1 receptor antagonists to identify compounds with activity at the peroxisome proliferator-activated receptor-γ (PPARγ) revealed a new series of ...

Novel imidazolyl and triazolyl substituted biphenyl compounds: synthesis and evaluation as nonsteroidal inhibitors of human 17alpha-hydroxylase-C17, 20-lyase (P450 17).

Bioorg. Med. Chem. 8(6) , 1245-52, (2000)

The synthesis of a new series of P450 17 inhibitors is described. The imidazol-1-yl compounds 5 showed strong inhibition of P450 17 rat and especially human enzyme, the most active compounds being 5ax...

The identification of potent and selective imidazole-based inhibitors of B-Raf kinase.

Bioorg. Med. Chem. Lett. 16(2) , 378-381, (2006)

A novel triarylimidazole derivative, SB-590885 (33), bearing a 2,3-dihydro-1H-inden-1-one oxime substituent has been identified as a potent and extremely selective inhibitor of B-Raf kinase.

Synonyms

5-Bromoindan-1-one
5-Bromo-1-indanone
1H-Inden-1-one, 5-bromo-2,3-dihydro-
1-Indanone, 5-bromo-
1H-Inden-1-one,5-bromo-2,3-dihydro
1-Indanone,5-bromo
5-bromoindane-1-one
5-Bromindan-1-on
5-bromo-2,3-dihydro-1H-indene-1-one
MFCD00082718
5-Brom-2,3-dihydro-1H-inden-1-on
5-bromo-2,3-dihydro-1H-inden-1-one
5-bromo-indanone
5-Bromoindanone
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