3916-12-9

Basic information

• Product Name: 1-benzylsulfanyl-N-(propan-2-ylideneamino)methanimidamide
• CAS NO: 3916-12-9
• Molecular Formula: C₁₁H₁₅N₃S
• Molecular Weight: 221.326
• Mol File: 3916-12-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1-benzylsulfanyl-N-(propan-2-ylideneamino)methanimidamide(CAS DataBase Reference)
• NIST Chemistry Reference: 1-benzylsulfanyl-N-(propan-2-ylideneamino)methanimidamide(3916-12-9)
• EPA Substance Registry System: 1-benzylsulfanyl-N-(propan-2-ylideneamino)methanimidamide(3916-12-9)

Safety Data

• Hazardous Substances Data: 3916-12-9(Hazardous Substances Data)

Usage

Explanation

The molecular formula represents the number of atoms of each element present in a molecule. In this case, the compound has 12 carbon (C) atoms, 15 hydrogen (H) atoms, 3 nitrogen (N) atoms, and 1 sulfur (S) atom.
2. Sulfanyl derivative

Explanation

A sulfanyl derivative is a compound that contains a sulfur atom bonded to a carbon atom through a single bond. This type of compound often has unique chemical properties and reactivity.
3. Propan-2-ylideneamino group

Explanation

The propan-2-ylideneamino group is a functional group consisting of a nitrogen atom double-bonded to a carbon atom, which is part of a three-carbon chain with a double bond between the first and second carbon atoms. This group is attached to the central carbon atom in the compound.
4. Central carbon atom

Explanation

Due to its unique structure and potential reactivity, 1-benzylsulfanyl-N-(propan-2-ylideneamino)methanimidamide may have various applications in different fields. These include organic synthesis (creating new compounds), pharmaceutical research (developing new drugs), and material science (creating new materials with specific properties).
6. Further research and investigation needed

Explanation

To fully understand the properties and potential applications of 1-benzylsulfanyl-N-(propan-2-ylideneamino)methanimidamide, additional research and investigation are required. This may involve studying its chemical reactivity, stability, and interactions with other compounds or materials.

Potential applications

Organic synthesis, pharmaceutical research, material science

Upstream product

• 100-44-7 benzyl chloride 
• 1752-30-3 Acetone thiosemicarbazone 
• 64-17-5 ethanol 
• 100-39-0 benzyl bromide 
• 79-19-6 thiosemicarbazide 
• 67-64-1 acetone 

Downstream Products

• 3922-43-8 Aceton-4--S-benzyl-isothiosemicarbazon 
• 77563-38-3 1-(isopropylideneamino)-5-p-chlorophenyl-2-S-benzyliso-4-thiobiuret 
• 80590-35-8 S-benzylthiosemicarbazide hydrochloride 
• 67-64-1 acetone 
• 7664-41-7 ammonia 
• 100-53-8 phenylmethanethiol 
• 77563-35-0 1-(isopropylideneamino)-5-o-tolyl-2-S-benzyliso-4-thiobiuret 
• 77563-39-4 1-(isopropylideneamino)-5-o-methoxyphenyl-2-S-benzyliso-4-thiobiuret 
• 77563-41-8 1-(isopropylideneamino)-5-p-ethoxyphenyl-2-S-benzyliso-4-thiobiuret 
• 77563-40-7 1-(isopropylideneamino)-5-p-methoxyphenyl-2-S-benzyliso-4-thiobiuret 
• 77563-34-9 1-(isopropylideneamino)-5-phenyl-2-S-benzyliso-4-thiobiuret 
• 77563-37-2 1-(isopropylideneamino)-5-o-chlorophenyl-2-S-benzyliso-4-thiobiuret 
• 3922-45-0 Aceton-4-

Relevant articles and documents

Some 3-arylimino-5(isopropylidene hydrazono-N)-1,2,4-dithiazolidines : Oxidative Debenzylation of 1-(isopropylideneamino)-5-aryl-2-S-benzyliso-4-thiobiurets

The synthesis of 3-arylimino-5-(isopropylidenehydrazono-N)-1,2,4-dithiazolidines has been described by the oxidative debenzylation of the corresponding 1-(isopropylideneamino)-5-aryl-2-S-benzyliso-4-thiobiurets.These compounds have been characterized by the direct oxidation of the corresponding 2,4-dithiobiurets and also by i.r. spectra.