66977-99-9

Basic information

• Product Name: 6-BROMO-1-HEXYNE
• Synonyms: 5-HEXYNE BROMIDE;6-BROMO-1-HEXYNE;1-BROMO-5-HEXYNE;6-Bromohex-1-yne;1-Hexyne, 6-bromo-
• CAS NO: 66977-99-9
• Molecular Formula: C₆H₉Br
• Molecular Weight: 161.04
• Mol File: 66977-99-9.mol
• Article Data: 9

Chemical Properties

• Boiling Point: 53-55 °C(Press: 10 Torr)
• Appearance: /
• Density: 1.293±0.06 g/cm3(Predicted)
• CAS DataBase Reference: 6-BROMO-1-HEXYNE(CAS DataBase Reference)
• NIST Chemistry Reference: 6-BROMO-1-HEXYNE(66977-99-9)
• EPA Substance Registry System: 6-BROMO-1-HEXYNE(66977-99-9)

Safety Data

• Hazardous Substances Data: 66977-99-9(Hazardous Substances Data)

Upstream product

• 928-90-5 5-hexyl-1-ol 
• 110-52-1 1,4-dibromo-butane 
• 1066-26-8 sodium acetylide 
• 76911-01-8 5-hexynyl p-toluenesulfonate 

Downstream Products

• 1623807-79-3 1-(4-(1-tosyl-1H-1,2,3-triazol-4-yl)butyl)-1H-indole 
• 1623807-92-0 (Z)-N-((8,9-dihydro-6H-azepino[1,2-a]indol-10(7H)-ylidene)methyl)-4-methylbenzenesulfonamide 
• 1623807-93-1 (E)-N-((8,9-dihydro-6H-azepino[1,2-a]indol-10(7H)-ylidene)methyl)-4-methylbenzenesulfonamide 
• 167693-19-8 2-(cyclopentylidenemethyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 
• 6097-08-1 2-(hex-5-yn-1-yl)isoindole-1,3-dione 
• 1903-27-1 cyclopentylidene acetic acid 
• 25712-33-8 anti-cyclohexane-1,2-diyldimethanol 
• 1218790-09-0 C₁₈H₃₄B₂O₄ 

Relevant articles and documents

TRIAZOLE DERIVATIVES AS P2Y14 RECEPTOR ANTAGONISTS

Described are compounds, which are antagonists of the P2Y14 receptor, for example, a compound of formula (I) in which ring A, R1,R2, R3, and n are as described herein. Also provided are dendron conjugates comprising the compounds, and methods of using the compounds, including a method of treating a disorder, such as inflammation, diabetes, insulin resistance, hyperglycemia, a lipid disorder, obesity, a condition associated with metabolic syndrome, and asthma, and a method of antagonizing P214 receptor activity in a cell.

Ni-Catalyzed Divergent Cyclization/Carboxylation of Unactivated Primary and Secondary Alkyl Halides with CO2

A user-friendly Ni-catalyzed reductive cyclization/carboxylation of unactivated alkyl halides with CO2 is described. The protocol operates under mild conditions with an excellent chemoselectivity profile and a divergent syn/anti selectivity pat