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80354-51-4

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80354-51-4 Usage

General Description

The chemical "2,4,5-trichlorophenyl (2-chloroethyl)nitrosocarbamate" is a synthetic organic compound that is used as a herbicide. It is known for its selective control of a wide range of annual broadleaf and grassy weeds in various crops, including soybeans, peanuts, and cotton. The compound works by inhibiting the growth of weeds through disrupting their photosynthesis process and causing cellular damage. It is toxic to aquatic organisms and can have harmful effects on the environment if not used properly. Additionally, it is important to follow safety precautions when handling this chemical, as it can cause irritation to the skin, eyes, and respiratory system.

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 articles and documents

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.

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