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2,2-dichloro-N,N-dipropylacetamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

39107-12-5

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39107-12-5 Usage

Physical state

Colorless liquid

Usage

Insect repellent and pesticide

Mechanism of action

Potent acetylcholinesterase inhibitor

Effect on the nervous system

Interferes with the breakdown of acetylcholine

Potential symptoms of overstimulation

Muscle tremors, seizures, respiratory failure

Regulatory status

Heavily regulated and restricted due to potential toxicity

Check Digit Verification of cas no

The CAS Registry Mumber 39107-12-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,1,0 and 7 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 39107-12:
(7*3)+(6*9)+(5*1)+(4*0)+(3*7)+(2*1)+(1*2)=105
105 % 10 = 5
So 39107-12-5 is a valid CAS Registry Number.

39107-12-5SDS

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 2,2-dichloro-N,N-dipropylacetamide

1.2 Other means of identification

Product number -
Other names N,N-dipropyl dichloroacetamide

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:39107-12-5 SDS

39107-12-5Downstream Products

39107-12-5Relevant academic research and scientific papers

Process for the preparation of imidazopyridines

-

, (2008/06/13)

A process for the preparation of an imidazopyridine which is a compound of formula (I) STR1 in which: Y denotes hydrogen, a halogen or a C1-4 alkyl group; X1 and X2 denote, independently of each other, hydrogen, a halogen or a C1-4 alkoxy, C1-6 alkyl, CF3, CH3 S, CH3 SO2 or NO2 group; and R1 and R2 denote, independently of each other, hydrogen or a C1-5 alkyl group, with the proviso that R1 and R2 do not both denote hydrogen, or a salt thereof; which process comprises reacting a compound of formula (V) STR2 wherein Y, X1, X2, R1 and R2 are as defined above, with a reducing agent and if desired converting the resulting compound of formula (I) into a salt, together with intermediates of formulae: STR3 The final products have useful pharmacological properties, e.g. as anxiolytics.

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