10191-60-3 | N-Cyanoimido-s,s-dimethyl-dithiocarbonate

Packsize	Purity	Availability	Price	Discounted Price
100g	98%	in stock	$19.00	$14.00
500g	98%	in stock	$80.00	$56.00

Description

• Catalog Number: AB72954
• Chemical Name: N-Cyanoimido-s,s-dimethyl-dithiocarbonate
• CAS Number: 10191-60-3
• Molecular Formula: C4H6N2S2
• Molecular Weight: 146.23384
• MDL Number: MFCD00009825
• SMILES: CSC(=NC#N)SC
• NSC Number: 145987

Computed Properties

• Complexity: 126
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 8
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 2
• XLogP3: 1.9

Upstream Synthesis Route

Dimethyl cyanocarbonimidodithioate, also known as a versatile reagent in chemical synthesis, is widely used in various organic reactions due to its unique properties. This compound is valuable in the synthesis of thioamide derivatives, as it serves as a crucial building block in the formation of organic molecules.One of the key applications of Dimethyl cyanocarbonimidodithioate is its role in the synthesis of thioamides, which are important intermediates in organic chemistry. Thioamides have diverse applications in pharmaceuticals, materials science, and agrochemicals. Dimethyl cyanocarbonimidodithioate enables the efficient conversion of amides to thioamides through a straightforward synthetic route, making it a valuable tool for organic chemists.Additionally, Dimethyl cyanocarbonimidodithioate can also participate in various multicomponent reactions, offering a convenient way to access structurally diverse compounds in a single synthetic step. This reagent's ability to introduce sulfur-containing functional groups makes it a versatile building block for the construction of complex molecular architectures.In summary, Dimethyl cyanocarbonimidodithioate is a versatile reagent with applications in the synthesis of thioamide derivatives and multicomponent reactions, making it a valuable tool for organic chemists seeking to efficiently access diverse organic molecules.

Literature

• (Z)-(1,3-Thia-zinan-2-ylideneamino)formo-nitrile.

  Acta crystallographica. Section E, Structure reports online 20090401

• [Synthesis and nNOS inhibitory activity of benzenealkyl isothiourea compounds].

  Yao xue xue bao = Acta pharmaceutica Sinica 20030801