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944903-27-9

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944903-27-9 Usage

Chemical structure

1-bromo-4-(prop-2-yn-1-yl)benzene consists of a benzene ring with a bromine atom attached to the 1-position and a prop-2-yn-1-yl group attached to the 4-position.

Functional groups

The compound contains a halogen (bromine), an alkyne (prop-2-yn-1-yl), and an aromatic ring (benzene).

Applications

It is commonly used in organic synthesis as a starting material for the preparation of various organic compounds and as a reagent in the production of pharmaceuticals and agrochemicals.

Physical properties

The compound is likely to be a liquid or solid at room temperature, depending on its exact molecular weight and structure.

Hazards

It is flammable and may cause irritation to the skin, eyes, and respiratory system upon exposure.

Safety precautions

It is important to handle this compound with care and use appropriate safety precautions, such as wearing gloves, goggles, and a lab coat, when working with it.

Reactivity

The compound may react with strong acids, bases, and oxidizing agents, so it should be stored and used away from these substances.

Stability

It is likely to be stable under normal laboratory conditions, but it should be stored in a cool, dry place and protected from light to prevent decomposition.

Solubility

The compound is likely to be soluble in organic solvents such as dichloromethane, ethyl acetate, and acetone.

Purity

The purity of the compound can be determined using techniques such as gas chromatography or high-performance liquid chromatography (HPLC).

Check Digit Verification of cas no

The CAS Registry Mumber 944903-27-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,4,9,0 and 3 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 944903-27:
(8*9)+(7*4)+(6*4)+(5*9)+(4*0)+(3*3)+(2*2)+(1*7)=189
189 % 10 = 9
So 944903-27-9 is a valid CAS Registry Number.

944903-27-9Downstream Products

944903-27-9Relevant articles and documents

Ruthenium-Catalyzed Propargylic Reduction of Propargylic Alcohols with Hantzsch Ester

Ding, Haowei,Sakata, Ken,Kuriyama, Shogo,Nishibayashi, Yoshiaki

supporting information, p. 2130 - 2134 (2020/06/08)

Ruthenium-catalyzed propargylic reduction of propargylic alcohols bearing a terminal alkyne moiety is accomplished by using Hantzsch ester as a nucleophilic hydride source. A variety of secondary and tertiary propargylic alcohols are reduced to the corresponding propargylic reduced products such as 1-alkynes in excellent yields. Some mechanistic studies indicate that ruthenium-allenylidene complexes may work as key reactive intermediates.

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