3-Cyclohexyl-1-propyne, 97%, Thermo Scientific Chemicals
3-Cyclohexyl-1-propyne, 97%, Thermo Scientific Chemicals
Thermo Scientific Chemicals

3-Cyclohexyl-1-propyne, 97%, Thermo Scientific Chemicals

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Quantity:
1 g
5 g
Catalog number B20505.03
also known as B20505-03
Price (USD)/ Each
46.40
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Quantity:
1 g
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Price (USD)/ Each
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3-Cyclohexyl-1-propyne, 97%, Thermo Scientific Chemicals
Catalog numberB20505.03
Price (USD)/ Each
46.40
-
Add to cart
Chemical Identifiers
CAS17715-00-3
IUPAC Name(prop-2-yn-1-yl)cyclohexane
Molecular FormulaC9H14
InChI KeyUARFKZSJGDQRLF-UHFFFAOYSA-N
SMILESC#CCC1CCCCC1
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SpecificationsSpecification SheetSpecification Sheet
FormLiquid
Refractive Index1.4560-1.4610 @ 20?C
Appearance (Color)Clear colorless
Assay (GC)≥96.0%

3-Cyclohexyl-1-propyne, is used as a pharmaceutical intermediate. It can be used to produce (5-bromo-4,4,5,5-tetrafluoro-pent-2-enyl)-cyclohexane at the temperature of 40°C. It will need reagents (NH4)2S2O8, HCO2Na·2H2O and solvent dimethylformamide with the reaction time of 3 hours. It is also used as organic synthesis intermediates.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
3-Cyclohexyl-1-propyne, is used as a pharmaceutical intermediate. It can be used to produce (5-bromo-4,4,5,5-tetrafluoro-pent-2-enyl)-cyclohexane at the temperature of 40°C. It will need reagents (NH4)2S2O8, HCO2Na·2H2O and solvent dimethylformamide with the reaction time of 3 hours. It is also used as organic synthesis intermediates.

Solubility
Slightly soluble in water.

Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Stable under recommended storage conditions. Keep away from strong oxidizing agents.
RUO – Research Use Only

General References:

  1. PH Lee.; S Kim.; A Park.; BC Chary. Gold (I)-Catalyzed Addition of Diphenyl Phosphate to Alkynes: Isomerization of Kinetic Enol Phosphates to the Thermodynamically Favored Isomers. Angewandte Chemie.2010122 (38), 6958-6961.
  2. F Taherirastgar.; L Brandsma. Conversion of Alkyl-and Arylallenes into 1-Alkynes Through Metallated Intermediates. Synthetic communications.199727 (23), 4035-4040.