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15090-26-3

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15090-26-3 Usage

Description

Propanoic acid, 3-(methoxymethylphosphinyl)-, methyl ester is an organic compound with a phosphinyl group attached to the third carbon of the propanoic acid backbone. It is characterized by its ester functional group, which is derived from the methyl ester of the propanoic acid. Propanoic acid, 3-(methoxymethylphosphinyl)-, methyl ester is known for its potential applications in various fields, particularly in the synthesis of specific chemical entities.

Uses

Used in Chemical Synthesis:
Propanoic acid, 3-(methoxymethylphosphinyl)-, methyl ester is used as a key intermediate in the synthesis of enantiomers of Phoshinothricin, also known as Glufosinate Ammonium (G596950). This herbicide is widely utilized in plant molecular biology and plant tissue culture for various purposes, including the selection of transformed cells and the control of unwanted plant growth.
Used in Plant Molecular Biology:
In the field of plant molecular biology, Propanoic acid, 3-(methoxymethylphosphinyl)-, methyl ester plays a crucial role in the development of herbicide-resistant plants. By synthesizing the enantiomers of Glufosinate Ammonium, this compound contributes to the advancement of genetic engineering techniques that enable the creation of plants with enhanced resistance to specific herbicides, thus improving crop yield and reducing the impact of weeds on agricultural productivity.
Used in Plant Tissue Culture:
Propanoic acid, 3-(methoxymethylphosphinyl)-, methyl ester is also employed in plant tissue culture for the selection and propagation of transformed cells. The synthesized enantiomers of Glufosinate Ammonium can be used as selective agents in tissue culture media, allowing for the identification and isolation of cells that have successfully incorporated the desired genetic traits. This process is essential for the development of new plant varieties with improved characteristics, such as higher yield, better disease resistance, and enhanced nutritional content.

Check Digit Verification of cas no

The CAS Registry Mumber 15090-26-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,0,9 and 0 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 15090-26:
(7*1)+(6*5)+(5*0)+(4*9)+(3*0)+(2*2)+(1*6)=83
83 % 10 = 3
So 15090-26-3 is a valid CAS Registry Number.

15090-26-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name methoxymethyl-(3-methoxy-3-oxopropyl)-oxophosphanium

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:15090-26-3 SDS

15090-26-3Relevant articles and documents

Synthesizing method of 3-(alkoxy methyl phosphoryl) propionic ester, analogue and phosphinothricin

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Paragraph 0018; 0019, (2016/12/22)

The invention discloses a synthesizing method of 3-(alkoxy methyl phosphoryl) propionic ester, analogue and phosphinothricin. The method is characterized in that 3-(methyl halogenated phosphoryl) propionyl halide is used as raw material, the 3-(methyl hal

Process for the preparation of phosphino compounds

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, (2008/06/13)

Process for the preparation of phosphino compounds Phosphorus-containing compounds of the formula (I) in which R1 and R2 are alkyl, alkoxy or optionally substituted phenyl, R3 and R5 are H, R, optionally substituted phenyl, ROCO--, RO--CO--RO--, halogen, CN, RO--, RO--RO--R-CO--, H2 NCO--, RNHCO-- or RRNCO--, in which R is alkyl, R4 and R6 have the same meaning as defined for R1 and R2 or are a divalent radical in which R7 is oxygen, NR* or sulfur, and R* is H, optionally substituted phenyl or alkyl, are precursors for plant protection agents and fire retardants. According to the invention they can be prepared in high yields and high purity by reacting a compound (R1)(R2)P--OR8, in which R8 is alkyl or optionally substituted phenyl, with an alkene of the formula R3 R4 C=CR5 R6 and at least an equimolar amount of aprotic organic substance such as alcohols, amines, phenols, thiophenols or anilines.

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