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7147-56-0

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7147-56-0 Usage

Type of compound

Carbamate derivative

Uses

Pesticide and herbicide

Mode of action

Inhibits the activity of the enzyme acetylcholinesterase

Effects on organisms

Affects the proper functioning of the nervous system in insects, fungi, and plants

Physical state

White solid at room temperature

Stability

Stable under normal conditions

Environmental impact

Toxic to aquatic organisms and may cause long-term adverse effects

Precautions

Should be handled and used with caution due to its potential environmental impact

Check Digit Verification of cas no

The CAS Registry Mumber 7147-56-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,4 and 7 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 7147-56:
(6*7)+(5*1)+(4*4)+(3*7)+(2*5)+(1*6)=100
100 % 10 = 0
So 7147-56-0 is a valid CAS Registry Number.

7147-56-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (ethylcarbamothioylamino)urea

1.2 Other means of identification

Product number -
Other names 1-ethyl-2-thiobiurea

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:7147-56-0 SDS

7147-56-0Relevant articles and documents

Heterocyclization of 1-aryl/alkyl-2-thiobiureas to 4-aryl/alkyl-3-substituted-Δ2-1,2,4-triazolin-5-ones

Suni,Nair, Vipin A,Joshua

, p. 2003 - 2009 (2007/10/03)

Synthesis of a range of 1,2,4-triazolin-5-ones has been carried out by thermally induced cyclization of 1-aryl/alkyl-2-alkyl isothiobiureas 4. The required isothiobiureas were generated in situ by the reaction of alkyl halides with 1-aryl/alkyl-2-thiobiureas 3 in acidic medium at reflux. The reaction proceeds after S-alkylation of the thiobiureas and is demonstrated by the isolation of the alkyl isothiobiurea intermediates and their subsequent acid catalyzed thermal cyclization.

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