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666963 Sigma-Aldrich

1-Heptyn-3-ol

97%

  • CAS Number 7383-19-9

  • Empirical Formula (Hill Notation) C7H12O

  • Molecular Weight 112.17

  •  MDL number MFCD00041597

  •  PubChem Substance ID 24884875

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Properties

Related Categories Alkynes, Building Blocks, Chemical Synthesis, Organic Building Blocks, Terminal More...
InChI Key   SHSFXAVQBIEYMK-UHFFFAOYSA-N
assay   97%
refractive index   n20/D 1.440
density   0.850 g/mL at 25 °C
storage temp.   2-8°C

Description

Packaging

1, 10 g in glass bottle

Safety & Documentation

Safety Information

Symbol 
Signal word 
Warning
Hazard statements 
RIDADR 
UN 1993C 3 / PGIII
WGK Germany 
3
Flash Point(F) 
138.2 °F
Flash Point(C) 
59 °C

Documents

Certificate of Analysis

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Protocols & Articles

Articles

Alkynes

Alkynes have been used for many years in the Sonogashira coupling reaction1 and related Castro-Stephens reaction,2 and have recently gained considerable interest in the Huisgen 1,3- dipolar cycloaddi...

Aldrich ChemFiles 2006, 6.6, 6.
Keywords: 1,3-Dipolar cycloaddition, Alkynylations, Asymmetric synthesis, Castro-Stephens coupling, Chemfiles, Cycloadditions, Dienylations, Hydrosilylations, Oxidations, Rearrangements, Sonogashira Coupling, Type, Vinylations

Functionalized Alkynes

Alkynes contain a highly versatile functional group that may be utilized for numerous reactions such as electrophilic additions of hydrogen, halogens, hydrogen halides, or water; metathesis; hydrobor...
Matthias Junkers
ChemFiles 2008, 8.1, 14.
Keywords: 1,3-Dipolar cycloaddition, Addition reactions, Building blocks, Click chemistry, Cycloadditions, Favorskii Reaction, Metathesis, Nucleophilic additions, Nucleophilic substitutions, Substitutions

Related Content

Alkynes and Acetylenic Building Blocks

We list over 600 alkyne building blocks, including a wide array of propargyl alcohols, acetylenic boron reagents, and halogenated substrates for cross-coupling. Additionally, many of these are termin...
Keywords: Building blocks, Coupling reactions, Cross couplings

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