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2-chloro-4-(4-chloro-phenyl)-5,5-dimethyl-[1,3,2]dioxaphosphinane 2-sulfide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

886044-03-7

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886044-03-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 886044-03-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,6,0,4 and 4 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 886044-03:
(8*8)+(7*8)+(6*6)+(5*0)+(4*4)+(3*4)+(2*0)+(1*3)=187
187 % 10 = 7
So 886044-03-7 is a valid CAS Registry Number.

886044-03-7Downstream Products

886044-03-7Relevant academic research and scientific papers

The synthesis and biological activities of N-(3-pyridylmethyl) N′-(trans-2-thio-4-substitutedphenyl-5,5-4dimethyl-1,3, 2-dioxaphosphinane-2-yl)thioureas

Shi, De-Qing,Feras, Abudhaim,Hamdan,Liu, Yi,Tan, Xiao-Song

, p. 1831 - 1838 (2007/10/03)

A series of novel title compounds were synthesized by the addition reaction of trans 2-isothiocyano-4-substitutedphenyl-5, 5-dimethyl-1,3,2- dioxaphosphinane 2-sulfide to 3-aminomethylpyridine or 2-chloro-5-amino methylpyridine. Their structures were conf

Asymmetric cyclic phosphorothonamides containing substituted pyridine

Shi, De-Qing,Feras, Abudhaim,Liu, Yi

, p. 2663 - 2673 (2007/10/03)

In order to find high-acitivity and low-toxicity pesticidal lead compounds, a type of novel, asymmetric cyclic phosphorothonamides containing substituted pyridine were synthesized via the condensation reactions of 2-chloro-4- substitutedphenyl-5,5-dimethy

Synthesis and fugicidal activities of 2-silatranyl propylamino-4-substitued phenyl(hydrogen)-5,5-dimethyl-1,3,2-dioxaphosphinanes-2-oxides (sulfides)

Wan, Shi-Guan,Yang, Xing-Yu,Yu, Yan,Liu, Chang

, p. 2813 - 2821 (2007/10/03)

Phosphoryl-aminopropyl-silatranes 4 were synthesized by nucleophilic reactions of 2-Cl-1,3,2- dioxaphosphinanes 2 with α-aminopropyl-silatrane 3, which was obtained by the cyclization reaction of triethanolamine and γ-aminopropyltriethoxysilane. The structures of the products were characterized by 1H NMR, 31P NMR, IR, MS, and elemental analyses. The target compounds 4 exhibited fungicidal activity. Copyright Taylor & Francis Inc.

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