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1-(5-bromopyridin-2-yl)propan-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1060812-89-6

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1060812-89-6 Usage

Functional groups

Ketone, pyridine ring, bromine atom, propyl group

Structure

A ketone derivative with a pyridine ring substituted with a bromine atom and a propyl group

Applications

a. Intermediate in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals
b. Building block in organic synthesis for the production of various heterocyclic compounds
c. Reagent in chemical reactions to introduce the 5-bromopyridin-2-ylpropan-1-one moiety into different molecules

Utility

Presence of bromine atom and pyridine ring allows for the creation of diverse structures with potential biological activity and industrial applications

Chemical properties

a. Reactivity with nucleophiles due to the presence of the ketone group
b. Reactivity with electrophiles due to the presence of the bromine atom
c. Aromaticity and resonance stabilization due to the pyridine ring

Boiling point

Depends on the specific conditions and purity of the compound

Melting point

Depends on the specific conditions and purity of the compound

Solubility

Generally soluble in organic solvents like ethanol, methanol, and dichloromethane

Toxicity

May be harmful if swallowed, inhaled, or absorbed through the skin

Reactivity

May react with strong oxidizing agents, reducing agents, or bases

Storage

Should be stored in a cool, dry, and well-ventilated area, away from heat and sources of ignition

Handling

a. Personal protective equipment (PPE) should be worn, including gloves, safety goggles, and a lab coat
b. Avoid inhalation, ingestion, and skin contact
c. Use in a fume hood or well-ventilated area to minimize exposure to vapors or dust

Disposal

Follow local, national, and international regulations for the disposal of chemical waste, including proper containment and labeling of hazardous materials

Check Digit Verification of cas no

The CAS Registry Mumber 1060812-89-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,6,0,8,1 and 2 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1060812-89:
(9*1)+(8*0)+(7*6)+(6*0)+(5*8)+(4*1)+(3*2)+(2*8)+(1*9)=126
126 % 10 = 6
So 1060812-89-6 is a valid CAS Registry Number.

1060812-89-6Downstream Products

1060812-89-6Relevant articles and documents

CARBOXYLIC ACID AROMATIC 1,2-CYCLOPROPYLAMIDES

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Paragraph 0798-0801, (2019/06/20)

The present invention relates to carboxylic acid aromatic 1,2-cyclopropylamides of general formula (I) as described and defined herein, to pharmaceutical compositions and combinations comprising said compounds and to the use of said compounds for manufacturing a pharmaceutical composition for the treatment or prophylaxis of a disease, in particular of neurogenic disorder, as a sole agent or in combination with other active ingredients.

CARBOXYLIC ACID AROMATIC AMIDES AS ANTAGONISTS OF BRADYKININ B1 RECEPTOR

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Page/Page column 133-134, (2018/07/29)

The present invention relates to carboxylic acid aromatic amides compounds of general formula (I) as described and defined herein, to pharmaceutical compositions and combinations comprising said compounds and to the use of said compounds for manufacturing

Enantioselective, catalytic trichloromethylation through visible-light-activated photoredox catalysis with a chiral iridium complex

Huo, Haohua,Wang, Chuanyong,Harms, Klaus,Meggers, Eric

supporting information, p. 9551 - 9554 (2015/08/18)

An enantioselective, catalytic trichloromethylation of 2-acyl imidazoles and 2-acylpyridines is reported. Several products are formed with enantiomeric excess of ≥99%. In this system, a chiral iridium complex serves a dual function, as a catalytically active chiral Lewis acid and simultaneously as a precursor for an in situ assembled visible-light-triggered photoredox catalyst.

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