21848-95-3

Basic information

• Product Name: N-TERTIARY BUTYL-N''-PHENYLCARBODIIMIDE
• Synonyms: N-TERTIARY BUTYL-N''-PHENYLCARBODIIMIDE;1-Phenyl-3-butylcarbodiimide, 95%
• CAS NO: 21848-95-3
• Molecular Formula: C₁₁H₁₄N₂
• Molecular Weight: 174.24
• Mol File: 21848-95-3.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• CAS DataBase Reference: N-TERTIARY BUTYL-N''-PHENYLCARBODIIMIDE(CAS DataBase Reference)
• NIST Chemistry Reference: N-TERTIARY BUTYL-N''-PHENYLCARBODIIMIDE(21848-95-3)
• EPA Substance Registry System: N-TERTIARY BUTYL-N''-PHENYLCARBODIIMIDE(21848-95-3)

Safety Data

• Hazardous Substances Data: 21848-95-3(Hazardous Substances Data)

Upstream product

• 2769-64-4 n-butyl isonitrile 
• 622-37-7 Phenyl azide 
• 62-53-3 aniline 
• 103-72-0 phenyl isothiocyanate 
• 6336-01-2 3-n-butyl-1-phenylthiourea 
• 3083-88-3 N-butyl-N'-phenylurea 

Downstream Products

• 10204-16-7 2-(butylamino)-3-phenylquinazolin-4(3H)-one 
• 1284224-18-5 N-butyl-1-phenyl-1H-2-aminobenzimidazole 
• 132783-02-9 Butyl-[(4R,5R)-4,5-dimethyl-3-phenyl-oxazolidin-(2Z)-ylidene]-amine 
• 132783-02-9 Butyl-[(4R,5S)-4,5-dimethyl-3-phenyl-oxazolidin-(2Z)-ylidene]-amine 
• 101835-26-1 N-butyl-3-phenyl-5-methyl-1,3-oxazolidin-2-imine 
• 101835-26-1 Butyl-[5-methyl-3-phenyl-oxazolidin-(2Z)-ylidene]-amine 
• 121518-17-0 Butyl-[4-methyl-3-phenyl-oxazolidin-(2Z)-ylidene]-amine 
• 85285-38-7 N-butyl-1-phenyl-1H-tetrazol-5-amine 
• 101306-22-3 C₁₂H₁₇N₃O₂ 
• 121485-60-7 Butyl-[5-methoxymethyl-3-phenyl-oxazolidin-(2Z)-ylidene]-amine 
• 121485-55-0 Butyl-[4-methoxymethyl-3-phenyl-oxazolidin-(2Z)-ylidene]-amine 
• 137146-08-8 2-butylimino-5-ethyl-3-phenyl-1,3-oxazolidine 
• 137146-04-4 2-butylimino-4-ethyl-3-phenyl-1,3-oxazolidine 
• 127704-13-6 3-phenyl-1,3-oxazin-2-(N-n-butyl)imine 

Relevant articles and documents

Convenient and Improved Synthesis of Unstable Carbodiimides

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A versatile thiouronium-based solid-phase synthesis of 1,3,5-triazines

A thiouronium-based solidphase synthesis of a 1,3,5-triazine scaffold has been developed. The key feature of the synthesis is the use of a readily accessible solid-supported thiouronium salt as a primary precursor for the stepwise assembly of the 1,3,5-tri-azine substrate. The sulfur linker employed in the synthesis is stable under both acidic and basic conditions and is versatile enough to provide access to monocyclic, bicyclic, and spirocyclic compounds with the 1,3,5-triazine scaffold. By using this synthetic strategy, a representative set of 79 compounds containing the 1,3,5-triazine scaffold were prepared.

DI-2-PYRIDYL THIONOCARBONATE. A NEW REAGENT FOR THE PREPARATION OF ISOTHIOCYANATES AND CARBODIIMIDES.

Reaction of amines with di-2-pyridyl thionocarbonate affords the corresponding isothiocyanates at room temperature, while reaction of N,N'-disubstituted thioureas with di-2-pyridyl thionocarbonate in the presence of 4-dimethylaminopyridine as a catalyst affords the corresponding carbodiimides in high yields.