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1-prop-2-en-1-yl-1,2-dihydro-5H-tetrazole-5-thione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

7624-33-1

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7624-33-1 Usage

Derivative of tetrazole

5-membered aromatic ring with 4 nitrogen atoms and 1 sulfur atom This describes the structure of the compound, which is based on a tetrazole ring, known for its stability and unique properties.

Use in organic synthesis

As a reagent and intermediate The compound is utilized in the synthesis of various organic compounds, acting as a reagent (a substance that initiates a reaction) and an intermediate (a temporary product formed during a reaction).

Application in medicinal chemistry

Preparation of pharmaceuticals and agrochemicals The compound is employed in the production of various drugs and agrochemicals, which are chemicals used in agriculture to protect crops from pests and diseases.

Potential antimicrobial and antifungal properties

These properties suggest that the compound may be effective in inhibiting the growth of microorganisms, such as bacteria and fungi, which can be beneficial in the development of new treatments for infections.

Unique structure and properties

The compound's distinctive structure and properties make it a valuable building block This highlights the importance of the compound in the synthesis of novel bioactive compounds, which can have potential applications in various fields, including medicine and agriculture.

Check Digit Verification of cas no

The CAS Registry Mumber 7624-33-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,6,2 and 4 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 7624-33:
(6*7)+(5*6)+(4*2)+(3*4)+(2*3)+(1*3)=101
101 % 10 = 1
So 7624-33-1 is a valid CAS Registry Number.

7624-33-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-prop-2-enyl-2H-tetrazole-5-thione

1.2 Other means of identification

Product number -
Other names 1-allyl-1,4-dihydro-tetrazole-5-thione

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:7624-33-1 SDS

7624-33-1Upstream product

7624-33-1Downstream Products

7624-33-1Relevant academic research and scientific papers

Mechanism of the zinc-catalyzed addition of azide ion to unsaturated compounds: Synthesis of 5-substituted 1Н-tetrazoles from nitriles and of 1-substituted 1Н-tetrazole-5-thiols from isothiocyanates

Myznikov,Vorona,Artamonova,Zevatskii, Yu. E.

, p. 731 - 738 (2017/05/29)

The mechanism of the formation of 5-substituted 1H-tetrazoles from organic nitriles and thiocyanates in the presence of NaN3 and ZnCl2 in aliphatic alcohols was studied. The results of this study allowed efficient methods of synthesis of substituted tetrazoles from nitriles, thiocyanates, and isothiocyanates to be proposed.

A facile one-pot synthesis of 1-substituted tetrazole-5-thiones and 1-substituted 5-alkyl(aryl)sulfanyltetrazoles from organic isothiocyanates

Han, Sam Yong,Lee, Je Woo,Kim, Hee-Jung,Kim, Yong-Joo,Lee, Soon W.,Gyoung, Young Soo

experimental part, p. 55 - 59 (2012/03/09)

Treatments of organic isothiocyanates (R-NCS) with NaN3 in the presence of pyridine in water at room temperature gave corresponding various organic tetrazole-thiones, [S=CN4(R)] (R = alkyl or aryl). Isolated products are obtained as white or yellow solids in good yields (76-97%). The molecular structure by X-ray diffraction study for one of products shows the proposed formation. In addition, one-pot synthesis of 1- substituted 5-alkyl(or aryl)sulfanyltetrazoles has been demonstrated. Addition of alkyl or aryl halides into the mixture of organic isothiocyanates, NaN3, and pyridine in water at room temperature exclusively formed 1- substituted 5-alkyl(or aryl)sulfanyltetrazoles (S-derivatives) in high yields.

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