51339-26-5 Usage
Description
(Phenyl)(3-trifluoromethylphenyl)methyl bromide, with the chemical formula C13H10BrF3, is a benzyl bromide derivative featuring a phenyl and a trifluoromethylphenyl group attached to the carbon atom. (phenyl)(3-trifluoromethylphenyl)methyl bromide is known for its stability and reactivity in organic reactions, largely due to its aromatic groups and the presence of the trifluoromethyl group, which can enhance the biological and pharmacological properties of synthesized molecules.
Uses
Used in Pharmaceutical Synthesis:
(Phenyl)(3-trifluoromethylphenyl)methyl bromide is utilized as a reagent in the organic synthesis of various biologically active molecules and pharmaceuticals. Its unique structure and functional groups contribute to the development of new drugs with improved efficacy and reduced side effects.
Used in Agrochemical Production:
(phenyl)(3-trifluoromethylphenyl)methyl bromide is also employed in the production of agrochemicals, where it serves as an intermediate for synthesizing compounds with pesticidal, herbicidal, or fungicidal properties. Its use in this industry helps to create more effective and targeted agrochemicals for agricultural applications.
Used in Fine Chemicals Industry:
(Phenyl)(3-trifluoromethylphenyl)methyl bromide is used as an intermediate in the synthesis of diverse organic compounds for the fine chemicals industry. Its bromide functional group makes it a versatile building block for creating specialty chemicals with specific applications in various markets, such as fragrances, dyes, and advanced materials.
Check Digit Verification of cas no
The CAS Registry Mumber 51339-26-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,3,3 and 9 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 51339-26:
(7*5)+(6*1)+(5*3)+(4*3)+(3*9)+(2*2)+(1*6)=105
105 % 10 = 5
So 51339-26-5 is a valid CAS Registry Number.
51339-26-5Relevant articles and documents
Tricyclic compounds, their production and use
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, (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.
SOLVOLYSES OF MONOSUBSTITUTED BENZHYDRYL BROMIDES. NUCLEOPHILIC SOLVENT INTERVENTION AND DEPENDENCE OF SOLVATATION ON THE EXTENT OF CHARGE DELOCALIZATION IN CATIONIC TRANSITION STATES
Liu, Kwang-Ting,Chin, Chien-Pu,Lin, Yen-Shyi,Tsao, Meng-Lin
, p. 6919 - 6922 (2007/10/02)
Solvolyses of monosubstituted benzhydryl bromides gave excellent linear correlations of logk with ?(1+) constants, and not with Y(BnBr) or Y(Br).Correlation analyses against corresponding logk of α-tert-butyl-(2-naphthyl)methyl bromide provided evidence for the importance of different extent of solvation in delocalized transition state and for nucleophilic solvent intervention in the solvolysis of benzhydryl systems.
