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28217-97-2

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28217-97-2 Usage

Uses

Chlormethiuron is used as a pesticide. An acaricide.

Check Digit Verification of cas no

The CAS Registry Mumber 28217-97-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,2,1 and 7 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 28217-97:
(7*2)+(6*8)+(5*2)+(4*1)+(3*7)+(2*9)+(1*7)=122
122 % 10 = 2
So 28217-97-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H13ClN2S/c1-7-6-8(11)4-5-9(7)12-10(14)13(2)3/h4-6H,1-3H3,(H,12,14)

28217-97-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name chloromethiuron

1.2 Other means of identification

Product number -
Other names N-(2-methyl-4-chlorophenyl)-N',N'-dimethylthiourea

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:28217-97-2 SDS

28217-97-2Downstream Products

28217-97-2Relevant articles and documents

Organophosphine-free copper-catalyzed isothiocyanation of amines with sodium bromodifluoroacetate and sulfur

Feng, Wei,Zhang, Xing-Guo

supporting information, p. 1144 - 1147 (2019/01/28)

A copper-catalyzed isothiocyanation of amines with sodium bromodifluoroacetate and sulfur in the absence of organophosphine has been established. This approach represents a simple and efficient one-pot synthesis of isothiocyanates, and features excellent functional group tolerance and the use of a cheap, safe and odorless sulfur source. Moreover, this process could directly provide isothiocyanate analogous bioactive molecules, thiocarbonyl-containing pesticides and facile construction of benzoxazole and benzimidazole frames.

Reaction of Thiocarbonyl Fluoride Generated from Difluorocarbene with Amines

Yu, Jiao,Lin, Jin-Hong,Xiao, Ji-Chang

, p. 16669 - 16673 (2017/12/07)

The reaction of thiocarbonyl fluoride, generated from difluorocarbene, with various amines under mild conditions is described. Secondary amines, primary amines, and o-phenylenediamines are converted to thiocarbamoyl fluorides, isothiocyanates, and difluoromethylthiolated heterocycles, respectively. Thiocarbamoyl fluorides were further transformed into trifluoromethylated amines by using a one-pot process. Thiocarbonyl fluoride is generated in situ and is rapidly fully converted in one pot under mild conditions; therefore, no special safety precautions are needed.

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