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α-Bromoethyltriphenylphosphonium bromide is a complex organic compound with the chemical formula C20H20BrP+Br-. It is a phosphonium salt, characterized by the presence of a phosphonium cation (P+) and a bromide anion (Br-). The molecule features a triphenylphosphonium cation, which consists of a central phosphorus atom bonded to three phenyl rings, and an α-bromoethyl group attached to the phosphorus. α-bromoethyltriphenylphosphonium bromide is often used as a reagent in organic synthesis, particularly in the formation of carbon-carbon bonds through the Wittig reaction, where it acts as a source of the bromomethyl anion. It is also known for its application in the synthesis of various pharmaceuticals and other organic compounds due to its ability to participate in a range of chemical transformations.

66070-22-2

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66070-22-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 66070-22-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,0,7 and 0 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 66070-22:
(7*6)+(6*6)+(5*0)+(4*7)+(3*0)+(2*2)+(1*2)=112
112 % 10 = 2
So 66070-22-2 is a valid CAS Registry Number.

66070-22-2Downstream Products

66070-22-2Relevant academic research and scientific papers

NOVEL REACTIONS OF PHOSPHONIUM YLIDES WITH PERHALOALKANES: FIRST EXAMPLES OF HALOPHILIC ATTACKS BY PHOSPHONIUM YLIDES AND A FACILE ROUTE TO α-HALOALKYLPHOSPHONIUM SALTS

Li, Xing-Ya,Hu, Jin-Shan

, p. 6317 - 6320 (2007/10/02)

Phosphonium ylides Ph3=CHR (R = H, CH3, C2H5, n-C3H7, n-C5H11) react readily with perhalofluoroalkanes to afford regiospecifically α-haloalkylphosphonium salts Ph3P+-CHXR Y- (X = I, Br, Cl) in good yields.These reactions reveal a new type of reactivity phosphonium ylides, i.e., the halophilic attack on C-X bonds, and may be useful for the regiospecific synthesis of substituted haloolefins via Wittig reaction.

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