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86147-22-0

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86147-22-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86147-22-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,1,4 and 7 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 86147-22:
(7*8)+(6*6)+(5*1)+(4*4)+(3*7)+(2*2)+(1*2)=140
140 % 10 = 0
So 86147-22-0 is a valid CAS Registry Number.

86147-22-0SDS

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 2-(chloromethyl)-1,3-dithiolane

1.2 Other means of identification

Product number -
Other names 2-CHLOROMETHYL-1,3-DITHIOLANE

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:86147-22-0 SDS

86147-22-0Downstream Products

86147-22-0Relevant articles and documents

Synthesis of 1,3-dithiolane-containing nitromethene compounds and their biological activity as insecticides

Li, Dongmei,Tian, Zhongzhen,Xu, Zhiping,Wang, Gaolei

, p. 2063 - 2070 (2013)

1,3-Dithiolane-containing nitromethylene derivatives, as candidates for screening as neonicotinoid insecticides, were synthesized by reaction of compound (4) with 1,2-ethanedithiol. Compounds 7a-g were obtained via Mannich reaction of (E)-1-((1,3-dithiolan-2-yl)methyl)-2-(nitromethylene)imidazolidine (6), primary amines and formaldehyde. The synthesized compounds were identified by 1H NMR, IR spectroscopy and elemental analysis. Preliminary bioassays indicated that most of the compounds had moderate insecticidal activity against Aphis craccivora. The relationship between molecular structure and biological activity is discussed.

METHODS FOR PREPARATION OF (4,6-DIHALO-PYRIMIDIN-5-YL)-ACETALDEHYDES

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Paragraph 0026; 0027, (2016/03/12)

This invention relates to the synthesis of chemical compounds and particularly to methods for the preparation of (4,6-dihalo-pyrimidin-5-yl)-acetaldehydes. The methods involve preparing a compound of the following general formula V from a compound of the following general formula IV through hydrolysis under the action of mercury dichloride and calcium carbonate, according to the following equation: wherein X is Cl or Br. The methods offer the benefits of use of highly available materials, high step yields, moderate reaction conditions, simply post-processing and purification, and suitability to industrialized production.

2-Methylene-1,3-dithiolane

Dahnke, Karl R.,Paquette, Leo A.

, p. 175 - 175 (2017/05/23)

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