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P-[[4-(4-Fluorophenyl)-6-(1-methylethyl)-2-[methyl(methylsulfonyl)amino]-5-pyrimidinyl]methyl]phosphonic acid dimethyl ester, commonly known as glyphosate, is a phosphonic acid herbicide used for controlling a wide range of broadleaf weeds and grasses. It functions by inhibiting the enzyme 5-enolpyruvylshikimate-3-phosphate synthase, which is crucial for the synthesis of aromatic amino acids in plants, ultimately leading to plant death. Glyphosate has been extensively utilized in agriculture and gardening, but its use has sparked debates due to potential health and environmental concerns.

1221497-92-2

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1221497-92-2 Usage

Uses

Used in Agricultural Industry:
P-[[4-(4-Fluorophenyl)-6-(1-methylethyl)-2-[methyl(methylsulfonyl)amino]-5-pyrimidinyl]methyl]phosphonic acid dimethyl ester is used as a herbicide for controlling broadleaf weeds and grasses in various crops, such as soybeans, corn, and cotton. Its application helps protect crops from weed competition, ensuring higher yields and better crop quality.
Used in Gardening and Landscaping:
P-[[4-(4-Fluorophenyl)-6-(1-methylethyl)-2-[methyl(methylsulfonyl)amino]-5-pyrimidinyl]methyl]phosphonic acid dimethyl ester is used as a weed control agent in gardens, lawns, and other landscaping areas. It helps maintain a clean and aesthetically pleasing environment by eliminating unwanted weeds without causing harm to the desired plants.
Used in Forestry and Rangeland Management:
P-[[4-(4-Fluorophenyl)-6-(1-methylethyl)-2-[methyl(methylsulfonyl)amino]-5-pyrimidinyl]methyl]phosphonic acid dimethyl ester is used as a vegetation management tool in forestry and rangeland areas. It helps control invasive plant species, promoting the growth of desired vegetation and maintaining the health of the ecosystem.
Used in Industrial and Residential Areas:
P-[[4-(4-Fluorophenyl)-6-(1-methylethyl)-2-[methyl(methylsulfonyl)amino]-5-pyrimidinyl]methyl]phosphonic acid dimethyl ester is used as a weed control agent in industrial and residential areas, such as along roadsides, railways, and utility corridors. Its application helps maintain a clean and safe environment by preventing the growth of unwanted vegetation that could cause hazards or obstruct visibility.

Check Digit Verification of cas no

The CAS Registry Mumber 1221497-92-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,1,4,9 and 7 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1221497-92:
(9*1)+(8*2)+(7*2)+(6*1)+(5*4)+(4*9)+(3*7)+(2*9)+(1*2)=142
142 % 10 = 2
So 1221497-92-2 is a valid CAS Registry Number.

1221497-92-2SDS

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 Dimethyl ({4-(4-fluorophenyl)-6-isopropyl-2-[methyl(methylsulfony l)amino]-5-pyrimidinyl}methyl)phosphonate

1.2 Other means of identification

Product number -
Other names dimethyl 2-oxo-3-(m-chlorophenoxy)propylphosphonate

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:1221497-92-2 SDS

1221497-92-2Relevant academic research and scientific papers

NOVEL PYRIMIDINE DERIVATIVE AND METHOD FOR PRODUCING HMG-CoA REDUCTASE INHIBITOR INTERMEDIATE

-

, (2011/08/08)

The problem to be solved of the present application is to provide a method for producing a novel pyrimidine derivative from an inexpensive compound which is industry-available with ease, and a method for producing an important intermediate of an HMG-CoA reductase inhibitor. The problem can be solved by, for example, reacting the compound (1) with the compound represented by (OR1) 3P to obtain the phosphonate ester (3) and reacting the phosphonate ester (3) with the compound (4) in the presence of a base to obtain an HMG-CoA reductase inhibitor intermediate (5).

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