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1-Ethynyl-1-cyclohexanol

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1-Ethynyl-1-cyclohexanol Basic information

Product Name:
1-Ethynyl-1-cyclohexanol
Synonyms:
  • 1-ETHYNYLCYCLOHEXANOL
  • 1-ETHYNYL-1-CYCLOHEXANOL
  • 1-ETHINYL-1-CYCLOHEXANOL
  • TIMTEC-BB SBB008829
  • (1-Hydroxycyclohexyl)ethyne
  • 1-ethvnvl-1-cvclohexanol
  • 1-Ethynyl-1-hydroxycyclohexane
  • 1-Ethynylcyclohexan-1-ol
CAS:
78-27-3
MF:
C8H12O
MW:
124.18
EINECS:
201-100-9
Product Categories:
  • Biphenyl & Diphenyl ether
  • Acetylenes
  • Acetylenic Alcohols & Their Derivatives
  • Alkynes
  • Organic Building Blocks
  • Terminal
  • Building Blocks
  • Chemical Synthesis
  • Organic Building Blocks
  • POSS
Mol File:
78-27-3.mol
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1-Ethynyl-1-cyclohexanol Chemical Properties

Melting point:
30-33 °C(lit.)
Boiling point:
180 °C(lit.)
Density 
0.967 g/mL at 25 °C(lit.)
vapor pressure 
<1 mm Hg ( 20 °C)
refractive index 
1.481-1.484
Flash point:
163 °F
storage temp. 
Store below +30°C.
solubility 
10 g/L (20°C)
form 
Liquid After Melting
pka
13.34±0.20(Predicted)
color 
Clear colorless to light yellow
PH
7 (1g/l, H2O, 20℃)
explosive limit
1.3-8.7%(V)
Water Solubility 
10 g/L (20 ºC)
BRN 
471404
InChIKey
QYLFHLNFIHBCPR-UHFFFAOYSA-N
LogP
1.49 at 25℃
CAS DataBase Reference
78-27-3(CAS DataBase Reference)
NIST Chemistry Reference
Cyclohexanol, 1-ethynyl-(78-27-3)
EPA Substance Registry System
Cyclohexanol, 1-ethynyl- (78-27-3)
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Safety Information

Hazard Codes 
Xn,Xi
Risk Statements 
21/22-36-36/37/38-20/21/22-36/38
Safety Statements 
36/37-36/37/39-26-36-22
RIDADR 
UN 2811 6.1/PG 3
WGK Germany 
1
RTECS 
GV9100000
Autoignition Temperature
365 °C
TSCA 
Yes
HazardClass 
6.1
PackingGroup 
III
HS Code 
29061900
Toxicity
LD50 orally in Rabbit: 583 mg/kg LD50 dermal Rabbit 973 mg/kg

MSDS

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1-Ethynyl-1-cyclohexanol Usage And Synthesis

Chemical Properties

Colorless liquid

Uses

Stabilization of chlorinated organic compounds, intermediate, corrosion inhibitor for mineral acids, medicine (sedative).

Uses

1-Ethynyl-1-cyclohexanol (ECHO) can undergo acetylation in the presence of a catalytic amount of ruthenium chloride at room temperature. It can be used to synthesize novel organotellurium(IV) compounds with potent inhibitory activity towards Cathepsin B. The polymerization of ECHO by transition metal catalysts leads to the formation of poly(ECHO). It can also react with transition metal hydride complexes to form vinyl derivatives by inserting into the M-H bonds.

Synthesis Reference(s)

Organic Syntheses, Coll. Vol. 3, p. 416, 1955
Synthetic Communications, 18, p. 131, 1988 DOI: 10.1080/00397918808077336

Flammability and Explosibility

Non flammable

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