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3-Pentanone, 2-bromo-2,4,4-trimethyl- is an organic compound with the chemical formula C8H15BrO. It is a halogenated ketone, characterized by the presence of a bromine atom and three methyl groups attached to the carbon skeleton. This colorless liquid has a molecular weight of 201.12 g/mol and a density of approximately 1.2 g/cm3. It is insoluble in water but soluble in organic solvents such as ethanol and acetone. The compound is used as a synthetic intermediate in the production of various chemicals and pharmaceuticals, and it is also employed as a reagent in organic synthesis. Due to its reactivity, it is important to handle 3-Pentanone, 2-bromo-2,4,4-trimethyl- with care, as it can be harmful if inhaled, ingested, or absorbed through the skin.

55007-44-8

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55007-44-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 55007-44-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,0,0 and 7 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 55007-44:
(7*5)+(6*5)+(5*0)+(4*0)+(3*7)+(2*4)+(1*4)=98
98 % 10 = 8
So 55007-44-8 is a valid CAS Registry Number.

55007-44-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-bromo-2,4,4-trimethylpentan-3-one

1.2 Other means of identification

Product number -
Other names 2-bromo-2,4,4-trimethyl-pentan-3-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:55007-44-8 SDS

55007-44-8Relevant academic research and scientific papers

Aminyl Radical Generation via Tandem Norrish Type i Photocleavage, β-Fragmentation: Independent Generation and Reactivity of the 2′-Deoxyadenosin- N6-yl Radical

Zheng, Liwei,Griesser, Markus,Pratt, Derek A.,Greenberg, Marc M.

, p. 3571 - 3580 (2017)

Formal hydrogen atom abstraction from the nitrogen-hydrogen bonds in purine nucleosides produces reactive intermediates that are important in nucleic acid oxidation. Herein we describe an approach for the independent generation of the purine radical resul

NOUVELLES METHODES DE DESHALOGENATION ET DE FORMATION D'ETHERS D'ENOL TRIMETHYLSILYLIQUES PAR ACTION DE iPr2NLi SUR QUELQUES α-MONOBROMO- ET α,α'-DIBROMOCETONES

Lion, Claude,Dubois, Jacques-Emile,Lebbar, Khadija

, p. 119 - 126 (2007/10/02)

Attempts to prepare 2-bromo-2,4-dimethyl,3-trimethylsiloxy 3-pentene reacting lithium diisopropylamide (LDA) with 2-bromo-2,4-dimethyl-3 pentanone have revealed two new reactions.After a few minutes quantitative yields are obtained of either the dehalogenated ketone (after hydrolysis) or the trimethylsilyl enol ether (after addition of trimethylsilyl chloride).These reactions are general and have been extended to other α-monobromoketones and α,α'-dibromoketones.In the latter case, the reaction is more complex and leads generally to dehalogenation or reduction products.

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