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α-(1,2,2-Trichlorovinyl)benzyl alcohol, also known as α-(1,2,2-trichloroethenyl)benzyl alcohol, is an organic compound with the chemical formula C9H9Cl3O. It is a colorless to pale yellow liquid with a molecular weight of 241.53 g/mol. α-(1,2,2-Trichlorethenyl)benzolmethanol is characterized by the presence of a benzyl alcohol group (C6H5CH2OH) and a 1,2,2-trichloroethenyl group (Cl3C=CH2). It is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly in the production of herbicides. Due to its reactivity and potential health and environmental concerns, it is important to handle this chemical with care, following proper safety protocols.

1769-47-7

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1769-47-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1769-47-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,6 and 9 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1769-47:
(6*1)+(5*7)+(4*6)+(3*9)+(2*4)+(1*7)=107
107 % 10 = 7
So 1769-47-7 is a valid CAS Registry Number.

1769-47-7Relevant academic research and scientific papers

Flash chemistry using trichlorovinyllithium: Switching the reaction pathways by high-resolution reaction time control

Nagaki, Aiichiro,Takahashi, Yusuke,Henseler, Andrea,Matsuo, Chika,Yoshida, Jun-Ichi

supporting information, p. 214 - 216 (2015/03/05)

High-resolution reaction time control in flow microreactors enables the reaction-pathway switching of trichlorovinyllithium generated by the H/Li exchange of trichloroethene. The method was successfully app lied to the synthesis of 1,1,2-trichloroalkenes,

Synthesis of functional derivatives of aryl trichlorovinyl (trichloroallyl) ketones via consecutive transformations of the carbonyl group

Potkin,Petkevich,Kletskov,Dikusar,Rozentsveig,Levkovskaya

, p. 1412 - 1421 (2015/02/19)

An efficient procedure have been developed for the selective reduction of the carbonyl group in phenyl trichlorovinyl ketone and aryl trichloroallyl ketones by the action of NaBH4 in propan-2-ol to obtain the corresponding alcohols. The hydroxy

Thermally Unstable Allenes, XII. (1,3,3-Trichloro-1,2-propadienyl)benzene

Roedig, Alfred,Detzer, Norbert

, p. 2374 - 2376 (2007/10/02)

The thermally unstable allene 4 is prepared from the ketone 1 via the intermediates 2 and 3.It dimerizes at room temperature to 5, whose structure is proven by permanganate degradation.

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