Cyclopropanemethanol, 98%, Thermo Scientific Chemicals
Element SearchElement SearchStructure SearchStructure Search
Cyclopropanemethanol, 98%, Thermo Scientific Chemicals
Thermo Scientific Chemicals

Cyclopropanemethanol, 98%, Thermo Scientific Chemicals

Have Questions?
Change viewbuttonViewtableView
Quantity:
25 g
5 g
100 g
ChemDexTry the chem dexTM web app
Catalog number A12567.14
also known as A12567-14
Price (USD)/ Each
72.40
-
Add to cart
Quantity:
25 g
Request bulk or custom format
Price (USD)/ Each
72.40
Add to cart
Cyclopropanemethanol, 98%, Thermo Scientific Chemicals
Catalog numberA12567.14
Price (USD)/ Each
72.40
-
Add to cart
Chemical Identifiers
CAS2516-33-8
IUPAC Namecyclopropylmethanol
Molecular FormulaC4H8O
InChI KeyGUDMZGLFZNLYEY-UHFFFAOYSA-N
SMILESOCC1CC1
View more
SpecificationsSpecification SheetSpecification Sheet
Assay (GC)≥97.5%
Appearance (Color)Clear colorless
Identification (FTIR)Conforms
Refractive Index1.4310-1.4350 @ 20?C
FormLiquid
Cyclopropanemethanol is used as an organic chemical synthesis intermediate.

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
Cyclopropanemethanol is used as an organic chemical synthesis intermediate.

Solubility
Fully miscible with water.

Notes
Stable under recommended storage conditions. Incompatible with oxidizing agents and acid chlorides.
RUO – Research Use Only

General References:

  1. Lewis Brewster Young; Walter S.Trahanovsky. Cerium(IV) oxidation of organic compounds. III. Preparation of cyclopropanecarboxaldehyde from cyclopropanemethanol. J. Org. Chem. 1967, 32, (7)2349-2350
  2. Yasunari Maeda; Takahiro Nishimura; Sakae Uemura. Vanadium-catalyzed isomerization of cyclopropanemethanols to homoallylic alcohols involving C-C bond cleavage. Chemistry Letters. 2005, 34, (3)380-381
  3. For conversion to cyclobutene by tert-butoxide-induced elimination from cyclobutyl tosylate, see: Org. Synth. Coll., 7, 117 (1990).