113439-90-0

Basic information

• Product Name: 4,4-DiMethyl-2-pentyn-1-aMine
• Synonyms: 4,4-DiMethyl-2-pentyn-1-aMine;4,4-Dimethylpent-2-yn-1-amine
• CAS NO: 113439-90-0
• Molecular Formula: C₇H₁₃N
• Molecular Weight: 111.18482
• Mol File: 113439-90-0.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 153.0±23.0 °C(Predicted)
• Appearance: /
• Density: 0.847±0.06 g/cm3(Predicted)
• PKA: 8.00±0.29(Predicted)
• CAS DataBase Reference: 4,4-DiMethyl-2-pentyn-1-aMine(CAS DataBase Reference)
• NIST Chemistry Reference: 4,4-DiMethyl-2-pentyn-1-aMine(113439-90-0)
• EPA Substance Registry System: 4,4-DiMethyl-2-pentyn-1-aMine(113439-90-0)

Safety Data

• Hazardous Substances Data: 113439-90-0(Hazardous Substances Data)

Upstream product

• 917-92-0 3,3-Dimethylbut-1-yne 
• 124316-00-3 1-<<(Triphenylphosphoranylidene)amino>methyl>benzotriazole 
• 88211-44-3 N-(methoxymethyl)-1,1,1-trimethyl-N-(trimethylsilyl)silanamine 
• 52323-99-6 1-bromo-4,4-dimethyl-2-pentyne 

Downstream Products

• 1161847-50-2 N-(4,4-dimethylpent-2-ynyl)-2-[2-methyl-3-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)phenyl]acetamide 
• 1161847-49-9 1-(4,4-dimethylpent-2-ynyl)-3-[2-methyl-3-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)phenyl]urea 

Relevant articles and documents

NOVEL IMIDAZO[1,2-A]PYRIDINE AND IMIDAZO[1,2-B]PYRIDAZINE DERIVATIVES

Imidazo[1,2-a]pyridine and imidazo[1,2-b]pyridazine derivatives which inhibit Btk and are useful for the treatment of auto-immune and inflammatory diseases caused by aberrant B-cell activation, e.g. arthritis.

Rhodium-Catalysed Reactions of Propargylamines with CO/H2. Formation of Pyrroles and Butenolides

Rhodium-catalysed reactions of (arylpropargyl)amines with CO/H2 give β-arylpyrroles in good yields.Reactions of (alkylpropargyl)amines gave alkylpyrroles together with butenolides which are formed in an unusual reaction that probably involves double carbonylation, reduction of one carbonyl function and removal of the amine function by hydrogenolysis.The single-crystal X-ray structure of 5-methyl-N,3-diphenylpyrrole-2-carboxamide is recorded.