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"2-[(3E)-3-(2-carbamothioylhydrazinylidene)butan-2-ylidene]hydrazinecarbothioamide" is a complex organic compound with the chemical formula C7H13N5S2. It is characterized by a hydrazinecarbothioamide core, which is a derivative of hydrazine with a thiocarbonyl group (C=S) attached. The compound features a 3-(2-carbamothioylhydrazinylidene)butan-2-ylidene moiety, indicating a butan-2-ylidene group with a 2-carbamothioylhydrazinylidene functional group. This group consists of a carbamoyl (urea-like) group connected to a thiocarbonyl group, which is in turn linked to a hydrazine moiety. The "E" configuration in the name suggests that the compound has a specific geometric arrangement around the double bond. This chemical is likely to be found in specialized applications due to its intricate structure, possibly in pharmaceuticals or as an intermediate in chemical synthesis.

7274-57-9

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7274-57-9 Usage

Chemical structure

2-[(3E)-3-(2-carbamothioylhydrazinylidene)butan-2-ylidene]hydrazinecarbothioamide The structure features a hydrazine derivative with a carbamothioylhydrazinylidene group attached to a butan-2-ylidene group.

Type of compound

Hydrazine derivative It is a compound derived from hydrazine (N2H4), which is a key component in the synthesis of various pharmaceuticals and pesticides.

Functional groups

Carbamothioylhydrazinylidene and carbothioamide These functional groups contribute to the compound's potential applications in medicinal chemistry, as they are important in the design of biologically active molecules.

Potential applications

Medicinal chemistry The compound's hydrazine and carbothioamide functionalities make it a promising candidate for the development of new drugs or materials with important applications in various fields.

Research potential

Further investigation into the properties and uses Studying 2-[(3E)-3-(2-carbamothioylhydrazinylidene)butan-2-ylidene]hydrazinecarbothioamide could lead to the creation of new drugs or materials with significant applications in multiple industries.

Check Digit Verification of cas no

The CAS Registry Mumber 7274-57-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,7 and 4 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 7274-57:
(6*7)+(5*2)+(4*7)+(3*4)+(2*5)+(1*7)=109
109 % 10 = 9
So 7274-57-9 is a valid CAS Registry Number.

7274-57-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name [(E)-[(3Z)-3-(carbamothioylhydrazinylidene)butan-2-ylidene]amino]thiourea

1.2 Other means of identification

Product number -
Other names 2,3-Bis-thiosemicarbazono-butan

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:7274-57-9 SDS

7274-57-9Downstream Products

7274-57-9Relevant academic research and scientific papers

IMAGING AGENTS

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Paragraph 0088, (2017/05/17)

The present invention provides certain thiosemicarbazone metal complexes which have advantageous properties in medical imaging. The thiosemicarbazone metal complexes can be safely and easily produced in real time, administered quickly after production, readily cross the blood-brain barrier, and may utilize a number of different radionuclides.

Heteronuclear NMR Spectroscopic Investigations of Gallium Complexes of Substituted Thiosemicarbazones Including X-Ray Crystal Structure, a New Halogen Exchange Strategy, and 18F Radiolabelling

Venkatachalam,Pierens,Bernhardt, Paul V.,Stimson,Bhalla,Lambert,Reutens

, p. 1033 - 1048 (2016/10/12)

Five thiosemicarbazone ligands have been synthesized, and their coordination chemistry with gallium was investigated. The reaction of these thiosemicarbazones with gallium chloride in alcohol solutions in the presence of a base yielded the corresponding p

Identification of differential anti-neoplastic activity of copper bis(thiosemicarbazones) that is mediated by intracellular reactive oxygen species generation and lysosomal membrane permeabilization

Stefani, Christian,Al-Eisawi, Zaynab,Jansson, Patric J.,Kalinowski, Danuta S.,Richardson, Des R.

, p. 20 - 37 (2015/09/07)

Bis(thiosemicarbazones) and their copper (Cu) complexes possess unique anti-neoplastic properties. However, their mechanism of action remains unclear. We examined the structure-activity relationships of twelve bis(thiosemicarbazones) to elucidate factors

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