Welcome to LookChem.com Sign In|Join Free
  • or
(3-fluorophenyl)phenylbromomethane, also known as 1-(bromomethyl)-3-fluorobenzene, is an organic compound with the chemical formula C13H10BrF. It is a colorless to pale yellow liquid that is soluble in organic solvents. (3-fluorophenyl)phenylbromomethane is characterized by the presence of a fluorine atom on the 3-position of the phenyl ring and a bromine atom attached to the methyl group, which is connected to the 1-position of the phenyl ring. It is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly in the production of compounds with potential applications in the treatment of diseases and pest control. Due to its reactivity, it is important to handle (3-fluorophenyl)phenylbromomethane with care, following appropriate safety measures to prevent exposure and potential health risks.

365-16-2

Post Buying Request

365-16-2 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

365-16-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 365-16-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,6 and 5 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 365-16:
(5*3)+(4*6)+(3*5)+(2*1)+(1*6)=62
62 % 10 = 2
So 365-16-2 is a valid CAS Registry Number.

365-16-2Relevant academic research and scientific papers

Kinetics of the solvolyses of fluoro-substituted benzhydryl derivatives: Reference electrofuges for the development of a comprehensive nucleofugality scale

Nolte, Christoph,Mayr, Herbert

supporting information; experimental part, p. 1435 - 1439 (2010/05/18)

A series of m-fluoro-substituted benzhydryl chloridcjs, bromides, mesylates and Losylates 1-X to 5-X were prepared and subjected to solvolysis reactions in various solvents. The observed first-order rate constants ks(25 °C) were found to follow the correlation equation log ks(25 °C) = Sf(Nf + Ef), which allowed us to determine the electrofugalily parameters Ef for these destabilized benzhydrylium cations and the nucleofugality parameters Nf, S f for a series of leaving group/ solvent combinations.

Synthesis and anticonvulsant activity of some cinnamylpiperazine derivatives

Hu, Chuan,Sun, Zhi-Gang,Wei, Cheng-Xi,Quan, Zhe-Shan

scheme or table, p. 661 - 664 (2011/11/29)

A series of cinnamylpiperazine derivatives was synthesized using different benzophenone as starting material. The structures of the compounds were proved by their IR, 1H-NMR spectroscopic data and mass spectra data. The anticonvulsant activities of these compounds were evaluated with maximal electroshock (MES) test and rotarod test with intraperitoneal injection on KunMing mice. Among all the flunarizine analogues, no one exhibited better anticonvulsant activity than flunarizine. Flunarizine (4i) exhibited anticonvulsant activity with ED50 of 38.1 mg/kg, TD50 of 164.3 mg/kg and PI of 4.3 through administration intraperitoneal, and with ED50 of 56.8 mg/kg, TD50 of 456.3 mg/kg and PI of 8.0 through oral administration.

Tricyclic compounds, their production and use

-

, (2008/06/13)

A compound of the formula: wherein R1 is H or a substituent; m is 1-3; Ar is an aromatic group which may be substituted; X is a bond or a divalent straight-chain group having 1-6 atoms which may be substituted; Y is —S—, —O—, or —N(R2— (R2 is H or a substituent group), Z is —N= or —C(R3)= (R3 is H or a hydrocarbon group), ring A is a benzene ring; ring B is a 5- to 7-membered ring which may be substituted, or a salt thereof is useful for eliciting a prostaglandin I2 receptor agonistic effect.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 365-16-2