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[2-Oxo-3-(4-trifluoromethylphenoxy)-propyl]-phosphonic acid dimethyl, a phosphonic acid derivative with the chemical formula C11H12F3O5P, is a versatile compound that features a phosphorus atom bonded to two methyl groups, a propyl group, and a phenyl group with a trifluoromethyl substitution. Its unique chemical properties make it a valuable asset across various industries.

1310798-67-4

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1310798-67-4 Usage

Uses

Used in Agricultural Industry:
[2-Oxo-3-(4-trifluoromethylphenoxy)-propyl]-phosphonic acid dimethyl is used as a pesticide or herbicide for its ability to inhibit the growth of certain plants and microorganisms, making it a valuable tool in controlling unwanted vegetation and protecting crops.
Used in Pharmaceutical Industry:
[2-Oxo-3-(4-trifluoromethylphenoxy)-propyl]-phosphonic acid dimethyl is utilized in the synthesis of pharmaceuticals, where its unique chemical properties contribute to the development of new drugs and therapeutic agents.
Used in Chemical Industry:
[2-Oxo-3-(4-trifluoromethylphenoxy)-propyl]-phosphonic acid dimethyl is also employed in the synthesis of other organic compounds, showcasing its versatility and applicability in the broader chemical industry.

Check Digit Verification of cas no

The CAS Registry Mumber 1310798-67-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,0,7,9 and 8 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1310798-67:
(9*1)+(8*3)+(7*1)+(6*0)+(5*7)+(4*9)+(3*8)+(2*6)+(1*7)=154
154 % 10 = 4
So 1310798-67-4 is a valid CAS Registry Number.

1310798-67-4Downstream Products

1310798-67-4Relevant academic research and scientific papers

Synthesis of (±) travoprost and its analogs

Mudduluru, Harikrishna,Hindupur, Rama M.,Dubey, Pramod K.,Madhavaram, Shankar,Tatini, Lakshmikumar,Subbaraju, Gottumukkala V.

, p. 234 - 241 (2012/04/18)

A new synthetic approach for the antiglaucoma agent, travoprost (1) has been developed in four steps from key intermediate (2). Key transformations include Horner-Wadsworth-Emmons reaction and separation of diastereomers to obtain (±) travoprost (1) and its analogs.

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