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7-(3-methoxyphenyl)-4,4-dimethyl-1,3-dioxo-3-ethoxybenzo[d][1,2]oxaphosphinine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1610696-96-2

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1610696-96-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1610696-96-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,1,0,6,9 and 6 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1610696-96:
(9*1)+(8*6)+(7*1)+(6*0)+(5*6)+(4*9)+(3*6)+(2*9)+(1*6)=172
172 % 10 = 2
So 1610696-96-2 is a valid CAS Registry Number.

1610696-96-2Upstream product

1610696-96-2Downstream Products

1610696-96-2Relevant academic research and scientific papers

Phosphaannulation by palladium-catalyzed carbonylation of C-H bonds of phosphonic and phosphinic acids

Shin, Seohyun,Jeong, Yeonseok,Jeon, Woo Hyung,Lee, Phil Ho

, p. 2930 - 2933 (2014)

An efficient phosphaannulation by Pd-catalyzed carbonylation of C-H bonds of phosphonic and phosphinic acids for the synthesis of oxaphosphorinanone oxides is reported. These compounds are novel phosphorus heterocyclic scaffolds, thus opening a new avenue to sequential C-C/C-O bond formation in one pot.

Novel benzo[d][1,2]oxaphosphorine derivatives and its synthetic method

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Paragraph 0066; 0156-0158, (2016/10/10)

The present invention relates to a novel benzo[d][1,2]oxaphosphorine derivative and a method for preparing the same. The benzo[d][1,2]oxaphosphorine derivative according to the present invention can be used as an important starting material or an intermediate applicable to a pharmaceutical industry and a crop protection industry by virtue of its physiological activity. In addition, the method for preparing a benzo[d][1,2]oxaphosphorine derivative according to the present invention comprises a step of carrying out carbon-hydrogen bond activation reaction of a benzyl phosphinic acid derivative by using a transition metal catalyst to form carbon-carbon and carbon-oxygen bonds with carbon monoxide. Thus, the method is advantageous in that various benzo[d][1,2]oxaphosphorine derivatives can be obtained in a one-pot process with high yield and low cost.

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