5-Bromoindanone

Modify Date: 2024-01-02 07:10:12

5-Bromoindanone Structure
5-Bromoindanone structure
Common Name 5-Bromoindanone
CAS Number 34598-49-7 Molecular Weight 211.06
Density 1.6±0.1 g/cm3 Boiling Point 303.7±31.0 °C at 760 mmHg
Molecular Formula C9H7BrO Melting Point 126-129 °C(lit.)
MSDS Chinese USA Flash Point 120.2±12.2 °C
Symbol GHS07
GHS07
Signal Word Warning

 Use of 5-Bromoindanone


5-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.

 Names

Name 5-bromo-2,3-dihydroinden-1-one
Synonym More Synonyms

 5-Bromoindanone Biological Activity

Description 5-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 Catalog

 Chemical & Physical Properties

Density 1.6±0.1 g/cm3
Boiling Point 303.7±31.0 °C at 760 mmHg
Melting Point 126-129 °C(lit.)
Molecular Formula C9H7BrO
Molecular Weight 211.06
Flash Point 120.2±12.2 °C
Exact Mass 209.968018
PSA 17.07000
LogP 2.86
Vapour Pressure 0.0±0.6 mmHg at 25°C
Index of Refraction 1.623
Storage condition -20°C

 Safety Information

Symbol GHS07
GHS07
Signal Word Warning
Hazard Statements H302-H312-H315-H319-H332-H335
Precautionary Statements P261-P280-P305 + P351 + P338
Personal Protective Equipment dust mask type N95 (US);Eyeshields;Gloves
Hazard Codes Xn:Harmful
Risk Phrases R22;R36/37/38
Safety Phrases S26-S36-S36/37/39
RIDADR NONH for all modes of transport
WGK Germany 3
HS Code 2914700090

 Synthetic Route

 Customs

HS Code 2914700090
Summary HS: 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

More Articles
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