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28249-27-6

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28249-27-6 Usage

Chemical Class

Carbamate pesticide

Function

Inhibits the activity of the enzyme acetylcholinesterase in insects

Mechanism of Action

Leads to paralysis and death in insects

Effective Against

Aphids, thrips, and mites

Usage

Agricultural and horticultural settings for protecting crops and plants

Toxicity

Can be toxic to humans and non-target organisms if not properly managed

Precaution

Handle and use with caution to minimize exposure and environmental impact

Check Digit Verification of cas no

The CAS Registry Mumber 28249-27-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,2,4 and 9 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 28249-27:
(7*2)+(6*8)+(5*2)+(4*4)+(3*9)+(2*2)+(1*7)=126
126 % 10 = 6
So 28249-27-6 is a valid CAS Registry Number.
InChI:InChI=1/C10H12ClNS2/c1-12(2)10(13)14-7-8-3-5-9(11)6-4-8/h3-6H,7H2,1-2H3

28249-27-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-chlorophenyl)methyl N,N-dimethylcarbamodithioate

1.2 Other means of identification

Product number -
Other names 4-chlorobenzyl dimethylcarbamodithioate

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:28249-27-6 SDS

28249-27-6Relevant articles and documents

Transition-Metal-Free C(sp3)–S Coupling in Water: Synthesis of Benzyl Dithiocarbamates Using Thiuram Disulfides as an Organosulfur Source

Peng, Han-Ying,Dong, Zhi-Bing

, p. 949 - 956 (2018/11/27)

A simple, highly efficient and environmentally benign method for the synthesis of benzyl dithiocarbamates was reported. Without addition of metal catalyst, a series of 34 benzyl dithiocarbamates were obtained in good to excellent yields by treating benzyl halides with tetraalkylthiuram disulfides in water. The protocol allows easy access to C(sp3)–S bond formation, features the advantages of easy performance, environmental friendliness, good to excellent yields, and good functional tolerance, showing potential value for the preparation of some biologically active compounds.

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