36668-76-5

Basic information

• Product Name: TERT-BUTYL CYANAMIDE
• Synonyms: TERT-BUTYL CYANAMIDE
• CAS NO: 36668-76-5
• Molecular Formula: C₅H₁₀N₂
• Molecular Weight: 98.15
• Mol File: 36668-76-5.mol
• Article Data: 11

Chemical Properties

• Appearance: /
• CAS DataBase Reference: TERT-BUTYL CYANAMIDE(CAS DataBase Reference)
• NIST Chemistry Reference: TERT-BUTYL CYANAMIDE(36668-76-5)
• EPA Substance Registry System: TERT-BUTYL CYANAMIDE(36668-76-5)

Safety Data

• Hazardous Substances Data: 36668-76-5(Hazardous Substances Data)

Upstream product

• 7204-48-0 N-(t-butyl)thiourea 
• 506-68-3 bromocyane 
• 75-64-9 tert-butylamine 
• 143-33-9 sodium cyanide 
• 506-77-4 cyanogen chloride 
• 73188-39-3 4-tert-butyl-4H-[1,2,4]oxadiazol-5-one 
• 590-42-1 tert-butyl isothiocyanate 
• 42956-75-2 N'-hydroxypivalimidamide 
• 630-19-3 pivalaldehyde 
• 637-91-2 2,2-dimethylpropionaldehyde oxime 
• 630-18-2 tert-butyl isocyanide 
• 73188-37-1 3,3-dimethyl-2-azabutanal oxime 
• 1118-12-3 1,1-dimethylethylurea 
• 119072-55-8 tert-butylisonitrile 

Downstream Products

• 1118-12-3 1,1-dimethylethylurea 
• 61705-46-2 C₁₄H₁₄F₃N₃O 
• 59772-93-9 1-tert-butyl-5-aminotetrazole 
• 1026091-77-9 C₅H₁₁N₅ 
• 1415921-15-1 2-tert-butylamino-6-phenyl-5-(3-phenylquinoxalin-2-yl)-4H-1,3-oxazin-4-one 
• 1350478-18-0 N-(tert-butyl)-N-(4-(trifluoromethyl)phenyl)cyanamide 
• 1310682-49-5 N-(tert-butoxycarbonyl)-N'-(3,4-dichlorophenyl)-N''-(1-tert-butyl-4-oxo-4,5-dihydro-1H-imidazol-2-yl)guanidine 
• 1310682-46-2 N-(3,4-dichlorophenyl)-N'-(1-tert-butyl-4-oxo-4,5-dihydro-1H-imidazol-2-yl)guanidine 
• 19520-09-3 N-tert.-Butyl-N'-<2-chlor-cyclohexyl>-harnstoff 
• 19520-16-2 N-<2-Chlor-2-phenyl-aethyl>-N-tert.-butyl-cyanamid 
• 65783-25-7 N-tert-Butyl-N'-(4-fluoro-phenyl)-guanidine 
• 65783-23-5 N-tert-Butyl-N'-(3-fluoro-phenyl)-guanidine 
• 76758-10-6 tert-Butyl-[5-(4-nitro-phenyl)-oxazol-2-yl]-amine 
• 122975-92-2 2-tert-Butylamino-6-p-tolyl-[1,3]oxazin-4-one 

Relevant articles and documents

SO2F2-Mediated one-pot cascade process for transformation of aldehydes (RCHO) to cyanamides (RNHCN)

A simple, mild and practical cascade process for the direct conversion of aldehydes to cyanamides was developed featuring a wide substrate scope and great functional group tolerability. This method allows for transformations of readily available, inexpensive, and abundant aldehydes to highly valuable cyanamides in a pot, atom, and step-economical manner with a green nitrogen source. This protocol will serve as a robust tool for the installation of the cyanamide moiety in various complicated molecules.

Synthesis and Reactivity of N-Allenyl Cyanamides

N-Allenyl cyanamides have been accessed via a one-pot deoxycyanamidation-isomerization approach using propargyl alcohol and N-cyano-N-phenyl-p-methylbenzenesulfonamide. The utility of this novel class of allenamide was explored through derivatization, with hydroarylation, hydroamination, and cycloaddition protocols employed to access an array of cyanamide products that would be challenging to access using existing methods.

Palladium-catalyzed arylation of cyanamides

The cross-coupling of alkyl cyanamides with a number of aryl, heteroaryl, and vinyl halide and pseudohalide coupling partners has been developed via a modification of Pd-catalyzed amidation methods. The reactions proceed selectively under mild conditions with reasonable reaction times in moderate to excellent yields.