7420-35-1

Basic information

• Product Name: 3-bromobenzaldehyde thiosemicarbazone
• Synonyms: (2E)-2-(3-Bromobenzylidene)hydrazinecarbimidothioic acid
• CAS NO: 7420-35-1
• Molecular Formula: C₈H₈BrN₃S
• Molecular Weight: 258.1382
• Mol File: 7420-35-1.mol
• Article Data: 8

Chemical Properties

• Boiling Point: 372.502°C at 760 mmHg
• Flash Point: 179.083°C
• Density: 1.611g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.669
• CAS DataBase Reference: 3-bromobenzaldehyde thiosemicarbazone(CAS DataBase Reference)
• NIST Chemistry Reference: 3-bromobenzaldehyde thiosemicarbazone(7420-35-1)
• EPA Substance Registry System: 3-bromobenzaldehyde thiosemicarbazone(7420-35-1)

Safety Data

• Hazardous Substances Data: 7420-35-1(Hazardous Substances Data)

Upstream product

• 3132-99-8 m-bromobenzoic aldehyde 
• 79-19-6 thiosemicarbazide 
• 4346-94-5 thiosemicarbazide hydrochloride 

Downstream Products

• 300819-55-0 2-(2-(3-bromobenzylidene)hydrazinyl)thiazol-4(5H)-one 
• 108656-65-1 2-Amino-5-( 3-bromophenyl)-1,3,4-thiadiazole 

Relevant articles and documents

The design, synthesis, and: In vitro trypanocidal and leishmanicidal activities of 1,3-thiazole and 4-thiazolidinone ester derivatives

Chagas and leishmaniasis are both neglected tropical diseases, whose inefficient therapies have made them remain the cause for millions of deaths worldwide. Given this, we synthesized 27 novel 1,3-thiazoles and 4-thiazolidinones using bioisosteric and est

Effect of organic solvents on solvatochromic, fluorescence, and electrochemical properties of synthesized thiazolylcoumarin derivatives

In this present investigation, thiazolylcoumarin derivatives (5a–5k) were synthesized from thiosemicarbazide, ethyl acetoacetate, and naphthaldehyde through a multistep route. The formation of thiazolylcoumarin derivatives with bioactive scaffolds was con

PhI-Catalyzed Intramolecular Oxidative Coupling Toward Synthesis of 2-Amino-1,3,4-Thiadizoles

A highly efficient method for the synthesis of thiadiazole derivatives via intramolecular oxidative coupling of thiosemicarbazide, using the in situ generated hypervalent iodine(III) reagents is developed. The protocol can be carried out smoothly and provides a variety of thiadiazole derivatives in moderate to excellent yields. Graphical Abstract: A highly efficient method for the synthesis of thiadiazole derivatives via PhI-catalyzed intramolecular oxidative coupling of thiosemicarbazide has been developed.