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2,3-Dibromo-3-(2-fluorophenyl)propionic acid is a chemical compound with the molecular formula C9H7Br2FO2. It is a derivative of propionic acid, featuring two bromine atoms at the 2nd and 3rd carbon positions, and a 2-fluorophenyl group attached to the 3rd carbon. This organic compound is characterized by its unique structure, which combines the properties of halogenated and fluorinated compounds. It is a white crystalline solid and is used in various chemical reactions and synthesis processes, particularly in the pharmaceutical and agrochemical industries. Due to its complex structure, it is important to handle 2,3-Dibromo-3-(2-fluorophenyl)propionic acid with care, as it may have potential health and environmental impacts.

342-19-8

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342-19-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 342-19-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,4 and 2 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 342-19:
(5*3)+(4*4)+(3*2)+(2*1)+(1*9)=48
48 % 10 = 8
So 342-19-8 is a valid CAS Registry Number.

342-19-8Relevant academic research and scientific papers

Gas-solid reactions of single crystals: A study of the reaction of bromine with single crystals of trans-cinnamic acid and a range of its derivatives by infrared and Raman microspectroscopy

Jenkins, Samantha L.,Almond, Matthew J.,Hollins, Peter

, p. 1966 - 1970 (2005)

Single crystals of trans-cinnamic acid and of a range of derivatives of this compound containing halogen substituents on the aromatic ring have been reacted with 165 Torr pressure of bromine vapour in a sealed desiccator at 20°C for 1 week. Infrared and Raman microspectroscopic examination of the crystals shows that bromination of the aliphatic double bond, but not of the aromatic ring, has occurred. It is demonstrated also that the reaction is truly gas-solid in nature. A time-dependent study of these reactions shows that they do not follow a smooth diffusion-controlled pathway. Rather the reactions appear to be inhomogeneous and to occur at defects within the crystal. The reaction products are seen to flake from the surface of the crystal. It is shown, therefore, that these are not single crystal to single crystal transitions, as have been observed previously for the photodimerisation of trans-cinnamic acid and several of its derivatives. It is shown that there are no by-products of the reaction and that finely ground samples react to form the same products as single crystals. The Owner Societies 2005.

Synthesis of the Substituted Z-1-Bromo-1-alkenes and Arylacetylenes from 2,3-Dibromocarboxylic Acids

Matveeva,Erin,Kurz

, p. 1065 - 1067 (2007/10/03)

Stereoselectivity was studied of simultaneous debromination-decarboxylation of dibrominated cinnamic and acrylic acids. The best selectivity in formation of Z-vinyl bromides was achieved with the use of organic nitrogen bases. The 1-bromo-1-alkenes were converted into the corresponding acetylenes.

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