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2,4,5-Trichlorophenyl (2-chloroethyl)nitrosocarbamate is a synthetic organic compound that functions as a potent herbicide. It is characterized by its ability to selectively control a broad spectrum of annual broadleaf and grassy weeds across various crops. 2,4,5-trichlorophenyl (2-chloroethyl)nitrosocarbamate exerts its herbicidal action by inhibiting the photosynthesis process in weeds, leading to cellular damage and ultimately, the death of the weed. However, it is also recognized for its potential environmental impact and toxicity to aquatic organisms, necessitating careful handling and application to minimize ecological harm.

80354-51-4

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80354-51-4 Usage

Uses

Used in Agricultural Applications:
2,4,5-Trichlorophenyl (2-chloroethyl)nitrosocarbamate is used as a herbicidal agent for the selective control of a wide range of annual broadleaf and grassy weeds in various crops such as soybeans, peanuts, and cotton. It is applied to effectively manage weed populations that compete with these crops for resources, thereby enhancing crop yield and quality.
Used in Environmental Management:
While the primary use of 2,4,5-trichlorophenyl (2-chloroethyl)nitrosocarbamate is in agriculture, its application also has implications for environmental management. It is crucial to follow safety guidelines and best practices in its use to mitigate the risk of harmful effects on non-target organisms, particularly aquatic life, and to prevent contamination of water bodies and soil.
Used in Safety Precautions:
Given its potential toxicity and irritancy, 2,4,5-trichlorophenyl (2-chloroethyl)nitrosocarbamate is also used as a reminder of the importance of safety precautions in agricultural and chemical handling contexts. This includes the use of personal protective equipment to prevent skin, eye, and respiratory system irritation, as well as the implementation of measures to minimize the chemical's impact on the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 80354-51-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,3,5 and 4 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 80354-51:
(7*8)+(6*0)+(5*3)+(4*5)+(3*4)+(2*5)+(1*1)=114
114 % 10 = 4
So 80354-51-4 is a valid CAS Registry Number.

80354-51-4SDS

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 (2,4,5-trichlorophenyl) N-(2-chloroethyl)-N-nitrosocarbamate

1.2 Other means of identification

Product number -
Other names N-(chloro-2 ethyl)N-nitrosocarbamate de trichloro-2,4,5 phenyle

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:80354-51-4 SDS

80354-51-4Relevant academic research and scientific papers

Synthesis and preliminary in vitro evaluation of antitumor nitrosoureido cholesterol derivatives

Elkihel,Gelin,Letourneux

, p. 190 - 194 (2007/10/02)

A new class of chloroethyl nitrosourea analogues of cholesterol has been synthetized from the corresponding 7-amino and 7-aminoalkylcholesterol derivatives. Compounds III-V inhibited L1210 cell growth in culture much more effectively than N,N'-bis(2-cgloroethyl)-N'-nitrosourea (BCNU) after 48 h incubation. Stability and cytotoxic activity of these prodrugs are promising for brain tumor treatments and as lymphotropic vectors for tumor cells spreading along the lymphatic pathways.

Activated N-Nitrosocarbamates for Regioselective Synthesis of N-Nitrosoureas

Martinez, Jean,Oiry, Joel,Imbach, Jean Louis,Winternitz, Francois

, p. 178 - 182 (2007/10/02)

A practical and convenient method for synthesizing antitumor compounds, N-alkyl-N-nitrosoureas, regioselectively nitrosated on the nitrogen atom bearing the alkyl group is proposed.N-Alkyl-N-nitrosocarbamates are interesting intermediates in these syntheses and yield, by reaction with amino compounds, the regioselectively nitrosated N-alkyl-N-nitrosoureas.As an interesting example, N,N'-biscystamine, a new attractive oncostatic derivative, has been prepared.The cytotoxic activity of these various compounds were tested on L1210 leukemia.

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