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o-Chlorophenylphosphonous dichloride is an organophosphorus compound with the chemical formula C6H4Cl3OP. It is a colorless to pale yellow liquid that is soluble in organic solvents. o-chlorophenylphosphonous dichloride is primarily used as an intermediate in the synthesis of various organophosphorus compounds, such as pesticides and flame retardants. It is also employed in the preparation of pharmaceuticals and other specialty chemicals. Due to its reactivity, o-chlorophenylphosphonous dichloride requires careful handling and storage to prevent unwanted reactions or hazards.

1004-78-0

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1004-78-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1004-78-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,0 and 4 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1004-78:
(6*1)+(5*0)+(4*0)+(3*4)+(2*7)+(1*8)=40
40 % 10 = 0
So 1004-78-0 is a valid CAS Registry Number.

1004-78-0Upstream product

1004-78-0Relevant academic research and scientific papers

AlCl3-catalyzed C-H p hosphination of benzene: A mechanistic study

Duan, Haodong,Gao, Jun,Guo, Ge,Han, Yuxi,Leng, Kangwei,Li, Xinjin,Wang, Zhongwei,Xu, Xiaolei,Yu, Qing

, (2021/01/06)

The characteristics of the reaction for the preparation of dichlorophenylphosphine (DCPP) via benzene and PCl3 in the presence of AlCl3 were studied. Some unique characteristics were observed when a catalytic amount of AlCl3 was used. Namely, more than one mole of DCPP was obtained per mole AlCl3, the reaction solution was layered, and DCPP could be directly separated. Our mechanistic study showed that benzene reacted with PCl3 to form DCPP-AlCl3, and DCPP-AlCl3 dissociated into DCPP and AlCl3, continuing to catalyze this reaction. This resulted in the high catalytic efficiency of AlCl3. The layering of the reaction solution was caused by the immiscibility of DCPP-AlCl3 with the raw materials, greatly facilitating the dissociation process of DCPP-AlCl3. The formation of diphenylphosphorus chloride (DPC) was due to a continuous Friedel-Crafts reaction between DCPP and benzene. DPC cooperated with AlCl3 to form the stable coordination compound DPC-AlCl3 that did not dissociate and was responsible for the deactivation of AlCl3.

DIARYLPHOSPHINIC AZIDES. PHOTOCHEMICAL REACTIONS INCLUDING REARRANGEMENT IN METHANOL

Harger, Martin J.P.,Westlake, Sally

, p. 1511 - 1516 (2007/10/02)

On photolysis in methanol the diarylphosphinic azides Ar2P(O)N3 (Ar=phenyl, p-tolyl, p-anisyl, p-chlorophenyl) rearrange with loss of nitrogen to form (monomeric) metaphosphonimidates which are trapped by the solvent to give methyl NP-diarylphosphonamidates (7) (41-53percent).Diarylphosphinic amides (18-42percent) are also usually formed, presumably from (triplet) nitrenes.The limited evidence available suggests that the rearrangements take place directly from the photo-excited azides rather than via (singlet) nitrene intermediates.One of the products of rearrangement, methyl NP-di(p-chlorophenyl)phosphonamidate, suffers extensive photochemical dechlorination giving methyl N-phenyl-P-p-chlorophenylphosphonamidate.

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