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2-Methyl-dibromo-phosphine, also known as methyldibromophosphine, is a chemical compound with the formula CH3PBr2. It is a colorless, volatile, and highly toxic liquid that is sensitive to moisture and air. This organophosphorus compound is used as a precursor in the synthesis of various phosphorus-containing compounds, such as pesticides and flame retardants. Due to its reactivity and potential health hazards, it is essential to handle 2-methyl-dibromo-phosphine with extreme caution, using appropriate safety measures and equipment.

6460-26-0

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6460-26-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6460-26-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,4,6 and 0 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6460-26:
(6*6)+(5*4)+(4*6)+(3*0)+(2*2)+(1*6)=90
90 % 10 = 0
So 6460-26-0 is a valid CAS Registry Number.

6460-26-0Upstream product

6460-26-0Downstream Products

6460-26-0Relevant academic research and scientific papers

Facile Photochemical Synthesis of Benzylphosphines

Mueller, Gerhard,Waldkircher, Martin,Winkler, Martin

, p. 1606 - 1614 (2007/10/02)

Facile large-scale synthesis of the benzyl-dibromo-phosphines RPBr2 (R = C6H5CH2, 3,5-Me2C6H3CH2, 2-BrC6H4CH2) is accomplished by the photochemical reaction of toluene, mesitylene and 2-bromotoluene, respectively, with PBr3 in the absence of solvent.It the reactions are carried out up to 50percent completion the amount of by-products formed is remarkably low, rarely exceeding 10percent of the total amount of products formed.The selectivity of the photoreaction may be improved up to 98percent if it is carried out in a modified Soxhlet apparatus which allows the predominant irradiation of only the starting materials.The apparent limitations imposed by the low turnovers required to achieve good products formed in a short period of time and by the easy recovery of unreacted starting material by distillation.Thus in the case of 2-BrC6H4CH2PBr2, in a typical run 94 g (261 mmol) of product may be isolated after 2.5 h of irradiation of 970 mmol of 2-BrC6H5CH3 and 1.39 mol of PBr3.In this case the turnover is 32percent, the isolated yield 27percent, and the by-product 2-methylphenyl-dibromo-phosphine only amounts to less than 2percent.The benzyl-dibromo-phosphines are easily methylated with two equivalents of MeMgCl to give the respective benzyl-dimethyl-phosphines in 79-93percent yield.Tertiary benzylphosphines MePRR' (R = 2-BrC6H4CH2, R' = Me3SiCH2; R = R' = 2-BrC6H4CH2) are obtained in easy one-pot syntheses by consecutive reactions of 2-BrC6H4CH2PBr2 with Me3SiCH2MgCl and MeMgCl, and with 2-BrC6H4CH2MgBr and MeMgCl, respectively. - Keywords: Benzylphosphines, Photochemical Synthesis

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