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Phosphonic acid, [(dimethylphenylsilyl)methyl]-, diethyl ester, also known as (dimethylphenylsilylmethyl)phosphonic acid diethyl ester, is a complex organic compound with the chemical formula C14H23O3PSi. It is a colorless liquid that is soluble in common organic solvents. Phosphonic acid, [(dimethylphenylsilyl)methyl]-, diethyl ester is characterized by the presence of a phosphonic acid group, a dimethylphenylsilyl group, and two ethyl ester groups. It is synthesized through the reaction of dimethylphenylsilylmethylphosphonic acid with ethanol in the presence of a catalyst. This chemical is primarily used in the synthesis of various organophosphorus compounds and as a reagent in organic chemistry. Due to its complex structure and reactivity, it is an important intermediate in the preparation of pharmaceuticals, agrochemicals, and other specialty chemicals.

727-15-1

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727-15-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 727-15-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,2 and 7 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 727-15:
(5*7)+(4*2)+(3*7)+(2*1)+(1*5)=71
71 % 10 = 1
So 727-15-1 is a valid CAS Registry Number.

727-15-1Downstream Products

727-15-1Relevant academic research and scientific papers

PHOSPHONATES α-SILYLES (RO)2P(O)CR1R2SiR3R4R5 ET α,α-DISILYLES (RO)2P(O)CR12; PREPARATION ET PROPRIETES

Savignac, Philippe,Teulade, Marie-Paule,Collignon, Noel

, p. 135 - 144 (2007/10/02)

Phosphonoalkylation of trisubstituted chlorosilanes in the presence of excess i-Pr2NLi has been examined to establish the steric and electrophilic properties of each silane.A similar sequence has been developed for the introduction of two Si(CH3)3 groups.The Si-C bond cleavage clearly demonstrates the protecting effect of trisubstituted silyl groups; but the silyl groups do not influence the formation of vinylphosphonates in the Peterson reaction.

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