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2-(propylcarbamothioyl)hydrazinecarboxamide, commonly known as prothidamide, is a carbamate chemical compound that functions as a fungicide. It is utilized in agriculture to manage and control various fungal diseases that affect crops. 2-(propylcarbamothioyl)hydrazinecarboxamide operates by inhibiting the enzyme chitin synthase, which is essential for the development of fungal cell walls, thereby disrupting the growth and reproduction of fungi.

7147-57-1

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7147-57-1 Usage

Uses

Used in Agricultural Applications:
2-(propylcarbamothioyl)hydrazinecarboxamide is used as a fungicide for the protection of a broad spectrum of crops, including fruits, vegetables, and ornamental plants. It is applied to control fungal diseases that can damage or destroy these plants, ensuring a healthy and productive yield.

Check Digit Verification of cas no

The CAS Registry Mumber 7147-57-1 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 7 respectively.
Calculate Digit Verification of CAS Registry Number 7147-57:
(6*7)+(5*1)+(4*4)+(3*7)+(2*5)+(1*7)=101
101 % 10 = 1
So 7147-57-1 is a valid CAS Registry Number.

7147-57-1SDS

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 (propylcarbamothioylamino)urea

1.2 Other means of identification

Product number -
Other names 1-carbamoyl-4-propyl thiosemicarbazide

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:7147-57-1 SDS

7147-57-1Downstream Products

7147-57-1Relevant academic research and scientific papers

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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