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13679-83-9

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13679-83-9 Usage

Chemical class

Neonicotinoid

Use

Insecticide

Function

Controls pests in crops like cotton, maize, and soybeans

Mechanism of action

Disrupts the nervous system of insects, leading to paralysis and death

Effectiveness

Highly effective against a wide range of pest species

Special property

Systemic action, meaning it can be absorbed and distributed throughout the plant, providing long-lasting protection

Concerns

Impact on non-target organisms, including pollinators, and potential role in the decline of bee populations

Restrictions

Use has been restricted in some countries

Alternatives

Exploring alternative pest control methods

Check Digit Verification of cas no

The CAS Registry Mumber 13679-83-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,6,7 and 9 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 13679-83:
(7*1)+(6*3)+(5*6)+(4*7)+(3*9)+(2*8)+(1*3)=129
129 % 10 = 9
So 13679-83-9 is a valid CAS Registry Number.

13679-83-9SDS

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 1-(4-methyl-1,3-thiazol-2-yl)propan-1-one

1.2 Other means of identification

Product number -
Other names 1-(4-methyl-thiazol-2-yl)-propan-1-one

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:13679-83-9 SDS

13679-83-9Downstream Products

13679-83-9Relevant articles and documents

Aerobic oxidation of secondary benzylic alcohols and direct oxidative amidation of aryl aldehydes promoted by sodium hydride

Wang, Xinbo,Wang, David Zhigang

supporting information; experimental part, p. 3406 - 3411 (2011/06/17)

We reported herein new reactivities and possible mechanistic implications of a simplest oxidant (NaH/air) uncovered on a broad range of useful transformations, including aerobic alcohol oxidations, allylic alcohol isomerizations and oxidations, cyclopropyl alcohol fragmentations, and direct aryl aldehyde oxidative amidations. These readily implementable transition-metal-free processes feature exceptional material accessibility, operational simplicity, and environmental compatibility, and add new dimensions to its synthetic utilities that are fairly robust yet had not previously been fully realized and systematically explored.

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