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β-D1-β-Phenylethyl chloride, also known as 1-(chloromethyl)-1-phenylethane, is an organic compound with the chemical formula C8H9Cl. It is a colorless liquid with a pungent odor and is soluble in organic solvents. β-d1-β-phenylethyl chloride is primarily used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. It is also employed in the production of β-phenylethylamine, which is a key component in the synthesis of certain psychoactive substances. Due to its reactivity, β-D1-β-phenylethyl chloride requires careful handling and is typically stored under controlled conditions to prevent unwanted reactions.

55153-07-6

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55153-07-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 55153-07-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,1,5 and 3 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 55153-07:
(7*5)+(6*5)+(5*1)+(4*5)+(3*3)+(2*0)+(1*7)=106
106 % 10 = 6
So 55153-07-6 is a valid CAS Registry Number.

55153-07-6Upstream product

55153-07-6Downstream Products

55153-07-6Relevant academic research and scientific papers

Conversion of a (sp3)C-F bond of alkyl fluorides to (sp 3)C-X (X = Cl, C, H, O, S, Se, Te, N) bonds using organoaluminium reagents

Terao, Jun,Begum, Shameem Ara,Shinohara, Yoshiaki,Tomita, Masahiro,Naitoh, Yoshitaka,Kambe, Nobuaki

, p. 855 - 857 (2007)

A simple method for the conversion of (sp3)C-F bonds of alkyl fluorides to (sp3)C-X (X = Cl, C, H, O, S, Se, Te, N) bonds has been achieved by the use of a hexane solution of organoaluminum reagents having Al-X bonds. The Royal Society of Chemistry.

Halogen-exchange reactions between alkyl fluorides and boron trihalides or tetrahalides. A convenient synthesis of alkyl halides from alkyl fluorides

Namavari, Mohammad,Satyamurthy, N.,Barrio, Jorge R.

, p. 89 - 93 (2007/10/02)

A simple and effective method for converting fluoroalkanes to their corresponding chloro-, bromo- and iodo-alkanes using commercially available boron trihalides and titanium tetrahalides is described. - Keywords: Halogen-exchange reactions; Alkyl fluorides; Boron trihalides; Titanium tetrahalides; NMR spectroscopy; Mass spectrometry

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