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36042-94-1

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36042-94-1 Usage

Description

DI-O-TOLYLCHLOROPHOSPHINE, also known as Chlorodi(o-tolyl)phosphine, is an organic compound that serves as a crucial raw material and intermediate in various chemical processes. It is characterized by its phosphorus-chlorine bond and two o-tolyl groups, which contribute to its reactivity and versatility in chemical synthesis.

Uses

Used in Organic Synthesis:
DI-O-TOLYLCHLOROPHOSPHINE is used as a reagent for the synthesis of various organic compounds. Its phosphorus-chlorine bond and o-tolyl groups make it a valuable building block in the creation of complex organic molecules.
Used in Pharmaceutical Industry:
DI-O-TOLYLCHLOROPHOSPHINE is used as an intermediate in the development of pharmaceutical products. Its unique chemical properties allow it to be a key component in the synthesis of new drugs and medications.
Used in Agrochemicals:
DI-O-TOLYLCHLOROPHOSPHINE is used as a precursor in the production of agrochemicals, such as pesticides and fertilizers. Its role in these applications is to provide the necessary chemical structure for the active ingredients to be effective.
Used in Dye Stuff:
DI-O-TOLYLCHLOROPHOSPHINE is used as a starting material in the synthesis of dyes and pigments. Its chemical properties enable the creation of a wide range of colors and shades, making it an essential component in the dye industry.

Purification Methods

It is purified by fractional distillation in a vacuum (b 179-183o/7mm, 253-257o/15mm,) and the distillate solidifies (m 36o, also reported is m 37o). [Weinberg J Org chem. 40 3586 1975, McEwen et al. J Am Chem Soc 100 7304 1978, Beilstein 16 H 769, 16 IV 970 for chlorodi(p-tolyl)phosphine.]

Check Digit Verification of cas no

The CAS Registry Mumber 36042-94-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,0,4 and 2 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 36042-94:
(7*3)+(6*6)+(5*0)+(4*4)+(3*2)+(2*9)+(1*4)=101
101 % 10 = 1
So 36042-94-1 is a valid CAS Registry Number.
InChI:InChI=1/C14H14ClP/c1-11-7-3-5-9-13(11)16(15)14-10-6-4-8-12(14)2/h3-10H,1-2H3

36042-94-1 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
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  • Alfa Aesar

  • (H25890)  Chlorodi(o-tolyl)phosphine, 98%   

  • 36042-94-1

  • 1g

  • 797.0CNY

  • Detail
  • Alfa Aesar

  • (H25890)  Chlorodi(o-tolyl)phosphine, 98%   

  • 36042-94-1

  • 5g

  • 3048.0CNY

  • Detail
  • Aldrich

  • (686697)  Chlorodi(o-tolyl)phosphine  

  • 36042-94-1

  • 686697-1G

  • 895.05CNY

  • Detail
  • Aldrich

  • (686697)  Chlorodi(o-tolyl)phosphine  

  • 36042-94-1

  • 686697-5G

  • 2,862.99CNY

  • Detail

36042-94-1Relevant articles and documents

SYNTHESIS AND PHYSICAL PROPERTIES OF CHLORODI(o-TOLYL)PHOSPHINE, LITHIUM DI(o-TOLYL)PHOSHIDE AND THE DIPHOSPHINE SERIES (o-TOLYL)2P(CH2)NP(o-TOYLYL) (n =1-4, 6,8)

Clark, Peter W.,Mulraney, Bernard J.

, p. 51 - 59 (1981)

The starting material chlorodi(o-tolyl)phosphine has been prepared by the reaction of phosphorus trichloride and the Grignard of o-chlorotoluene.The intermediate lithium di(o-tolyl)phosphide was obtained by the direct reaction of lithium metal and chlorod

Method for preparing diarylphosphoryl chloride compound

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Paragraph 0016-0017, (2018/06/15)

The invention discloses a method for preparing a diarylphosphochlorine compound and belongs to the field of organic synthesis. The method is as follows: the diarylphosphochlorine compound is preparedby reaction of triarylphosphine as a starting material with phosphorus trichloride in the presence of zinc trifluoromethanesulfonate as a catalyst and distillation. Compared with the prior art, the method has the advantages of high reaction yield and simple post-treatment, is particularly suitable for preparation of the diarylphosphochlorine compound with a substituent, and is more suitable for industrial production. The obtained diarylphosphochlorine compound can be used as a ligand for synthesizing metal catalysts, and is applied to the fields such as organic photoelectric materials and medicines.

TETRAMERISATION OF ETHYLENE

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, (2014/12/09)

A process for the tetramerisation of ethylene includes contacting ethylene with a catalyst under ethylene oligomerisation conditions. The catalyst comprises a source of chromium, a ligating compound, and an activator. The ligating compound includes a phosphine that forms part of a cyclic structure.

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