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5-BROMO-4-METHYL-2,3-DIHYDRO-1H-INDEN-1-ONE is a chemical compound characterized by its molecular formula C10H9BrO. It is a yellowish solid with a molecular weight of 227.08 g/mol. 5-BROMO-4-METHYL-2,3-DIHYDRO-1H-INDEN-1-ONE features a cyclic structure with a bromine atom and a methyl group attached to a 2,3-dihydro-1H-inden-1-one core, which makes it a versatile intermediate in organic chemistry reactions. Its unique structure and properties also suggest potential uses in medicinal and biological research.

903557-48-2

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903557-48-2 Usage

Uses

Used in Chemical Synthesis:
5-BROMO-4-METHYL-2,3-DIHYDRO-1H-INDEN-1-ONE is used as a building block in the synthesis of other organic compounds. Its unique structure allows it to be a versatile intermediate in various chemical reactions, contributing to the development of new organic compounds with diverse applications.
Used in Pharmaceutical Applications:
In the pharmaceutical industry, 5-BROMO-4-METHYL-2,3-DIHYDRO-1H-INDEN-1-ONE is used as a key intermediate in the development of new drugs. Its unique structure and properties make it a promising candidate for the synthesis of pharmaceutical compounds with potential therapeutic effects.
Used in Medicinal and Biological Research:
5-BROMO-4-METHYL-2,3-DIHYDRO-1H-INDEN-1-ONE is also utilized in medicinal and biological research. Its distinctive structure and properties provide opportunities for exploring its potential in various research areas, including drug discovery and development, as well as understanding its interactions with biological systems.

Check Digit Verification of cas no

The CAS Registry Mumber 903557-48-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,3,5,5 and 7 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 903557-48:
(8*9)+(7*0)+(6*3)+(5*5)+(4*5)+(3*7)+(2*4)+(1*8)=172
172 % 10 = 2
So 903557-48-2 is a valid CAS Registry Number.

903557-48-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1H-Inden-1-one, 5-bromo-2,3-dihydro-4-methyl-

1.2 Other means of identification

Product number -
Other names 5-BROMO-4-METHYL-2,3-DIHYDRO-1H-INDEN-1-ONE

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:903557-48-2 SDS

903557-48-2Downstream Products

903557-48-2Relevant articles and documents

HETEROBICYCLIC METALLOPROTEASE INHIBITORS

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Page/Page column 116-117, 122-123, (2008/12/05)

The present invention relates generally to heterobicyclic containing pharmaceutical agents, and in particular, to heterobicyclic metalloprotease inhibitor compounds. More particularly, the present invention provides a new class of heterobicyclic metalloprotease inhibiting compounds that exhibit an increased potency in relation to currently known metalloprotease inhibitors.

METALLOPROTEASE INHIBITORS

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Page/Page column 64, (2008/06/13)

The present invention relates to amide containing aromatic MMP inhibiting compounds with a mono-amide heteroaromatic group, of formulas I and II:

HETEROBICYCLIC METALLOPROTEASE INHIBITORS

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Page/Page column 144; 146, (2008/06/13)

The present invention relates generally to amide group containing pharmaceutical agents, and in particular, to amide containing heterobicyclic metalloprotease inhibitor compounds. More particularly, the present invention provides a new class of heterobicyclic MMP- 13 inhibiting compounds, that exhibit an increased potency in relation to currently known MMP- 13 inhibitors.

Multicyclic bis-amide MMP inhibitors

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Page/Page column 119-120, (2008/06/13)

The present invention relates generally to bis-amide group containing pharmaceutical agents, and in particular, to multicyclic bis-amide MMP-13 inhibitor compounds. More particularly, the present invention provides a new class of MMP-13 inhibiting compounds, containing a pyrimidinyl bis-amide group in combination with a heterocyclic moiety, that exhibit an increased potency and solubility in relation to currently known bis-amide group containing MMP-13 inhibitors.

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