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85909-36-0

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85909-36-0 Usage

General Description

1-(2-chloropropoxy)-2-(phenylmethyl)benzene is a chemical compound with the molecular formula C19H21ClO. It is a benzene derivative with a 2-chloropropoxy group attached to the benzene ring at the 1 position and a phenylmethyl group attached at the 2 position. 1-(2-chloropropoxy)-2-(phenylmethyl)benzene is used in the pharmaceutical and chemical industries for the synthesis of various organic compounds and intermediates. It may also have potential applications in the field of organic chemistry and drug development. Additionally, it is important to handle this compound with caution, as it may have potential health and environmental hazards.

Check Digit Verification of cas no

The CAS Registry Mumber 85909-36-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,9,0 and 9 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 85909-36:
(7*8)+(6*5)+(5*9)+(4*0)+(3*9)+(2*3)+(1*6)=170
170 % 10 = 0
So 85909-36-0 is a valid CAS Registry Number.
InChI:InChI=1/C16H17ClO/c1-13(17)12-18-16-10-6-5-9-15(16)11-14-7-3-2-4-8-14/h2-10,13H,11-12H2,1H3

85909-36-0Relevant articles and documents

A green synthetic benproperine phosphate in intermediates (by machine translation)

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Paragraph 0022; 0023; 0024, (2018/11/22)

A green synthetic benproperine phosphate in intermediates, which belongs to the technical field of pharmaceutical intermediates. The process in the phenol and benzyl alcohol benzylating reaction, the introduction of 1, 1, 3, 3 - [...] sulfonyl propylene (TTP)/hexafluoroisopropanol (HFIP) catalytic system, the steps of reaction to enhance the yield of 95% - 100%; after a series of reaction can obtain the target product benproperine phosphate, avoid the Al2 O3 First activated and reaction, the production process is greatly simplified, improving the selectivity, yield is greatly improved. In the substituted hydroxy substitution chlorine in the step into, the introduction of methyl dichloro silane, anhydrous ferric trichloride, ethylene glycol dimethyl ether replacing thionyl chloride, benzene and pyridine. No sulfur dioxide, hydrogen chloride and other corrosive contaminants. Reduces the environment pollution and difficulty of post-processing; and easy operation, processing is simple. The method greatly improves the yield, the cost is reduced, and the safety is improved, and the energy is saved, accord with the green reaction of modern chemical production requirement. (by machine translation)

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