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Phosphoramidochloridic acid, dimethyl-, ethyl ester, also known as O,O-dimethyl-N-(phosphonomethyl)glycine ethyl ester, is a chemical compound with the molecular formula C5H12ClNO5P. It is a derivative of phosphoramidochloridic acid, featuring a dimethylamino group and an ethyl ester group. Phosphoramidochloridic acid, dimethyl-, ethyl ester is primarily used as a herbicide, specifically as a selective post-emergence herbicide for controlling broadleaf and grassy weeds in various crops. It works by inhibiting the enzyme enolpyruvylshikimate-3-phosphate synthase (EPSPS) in plants, which is essential for the synthesis of aromatic amino acids and, consequently, for plant growth. The ethyl ester form of Phosphoramidochloridic acid, dimethyl-, ethyl ester is designed to enhance its solubility and absorption by plants, making it more effective in controlling weed growth.

2510-93-2

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2510-93-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2510-93-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,1 and 0 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2510-93:
(6*2)+(5*5)+(4*1)+(3*0)+(2*9)+(1*3)=62
62 % 10 = 2
So 2510-93-2 is a valid CAS Registry Number.

2510-93-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[chloro(ethoxy)phosphoryl]-N-methylmethanamine

1.2 Other means of identification

Product number -
Other names N,N-Dimethyl-amidophosphorsaeure-aethylester-chlorid

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:2510-93-2 SDS

2510-93-2Upstream product

2510-93-2Relevant academic research and scientific papers

PHOSPHORIC, PHOSPHONIC, AND PHOSPHINIC ACID AMIDES AS BASES

Matrosov, E. I.,Kryuchkov, E. E.,Nifantyev, E. E.,Kozachenko, A. G.,Kabachnik, M. I.

, p. 69 - 78 (2007/10/02)

Potentiometric titration in nitromethane, IR- and NMR-spectroscopy were used to study the processes of protonation and H-bonding for a number of phosphoric, phosphonic and phosphinic acid amides. 12N)nP(O)R23-n(R1=Me, Et; R2=EtO, Me, Et; n=1-3) including 1,3,2-dioxa-, 1,3,2-oxazaphospholane and phosphorinane derivatives>.It was shown that in these compounds the center of the highest basicity is the oxygen of the phosphoryl group.

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