58655-25-7

Basic information

• Product Name: C₆H₁₅N*C₈H₈BrNS₂
• Synonyms: C₆H₁₅N*C₈H₈BrNS₂
• CAS NO: 58655-25-7
• Molecular Weight: 363.386
• Mol File: 58655-25-7.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: C₆H₁₅N*C₈H₈BrNS₂(CAS DataBase Reference)
• NIST Chemistry Reference: C₆H₁₅N*C₈H₈BrNS₂(58655-25-7)
• EPA Substance Registry System: C₆H₁₅N*C₈H₈BrNS₂(58655-25-7)

Safety Data

• Hazardous Substances Data: 58655-25-7(Hazardous Substances Data)

Upstream product

• 75-15-0 carbon disulfide 
• 583-68-6 2-bromo-p-toluidine 
• 121-44-8 triethylamine 

Downstream Products

• 1189350-87-5 6-methyl-2-(p-tolylthio)-1,3-benzothiazole 
• 66644-79-9 2-Bromo-4-methylphenylthiourea 
• 1208070-80-7 2-bromo-4-methylphenylcyanamide 
• 19241-39-5 (2-bromo-4-methylphenyl)isothiocyanate 

Relevant articles and documents

A one-pot preparation of cyanamide from dithiocarbamate using molecular iodine

An efficient one-pot method for the synthesis of cyanamides from dithiocarbamate salts via a double desulfurization strategy using molecular iodine is disclosed. Dithiocarbamates, by the action of iodine yield isothiocyanates in situ, which on treatment with aqueous NH3 give thioureas. The thioureas so generated undergo further oxidative desulfurization with I2 giving corresponding cyanamides in good yields. Environmental benignity, cost effectiveness and high yields are the important attributes of this one pot procedure. The Royal Society of Chemistry 2009.

Intra- and Intermodular C-S bond formation using a single catalytic system: First direct access to arylthiobenzothiazoles

We have for the first time developed two llgand-assisted Cu(I)-catalyzed sequential Intra- and intermolecular 5-arylations leading to the direct synthesis of arylthiobenzothlazoles In one pot without an Inert atmosphere. Low catalyst loading, inexpensive