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1-(tetrahydrofuran-2-yl)ethanol is a chemical compound with the molecular formula C6H12O2. It is a colorless liquid that is soluble in water and has a molecular weight of 116.16 g/mol. 1-(tetrahydrofuran-2-yl)ethanol is characterized by a tetrahydrofuran ring fused to an ethyl group, which is further connected to a hydroxyl group. It is used as a solvent, a reagent in organic synthesis, and as a building block for the synthesis of various pharmaceuticals and specialty chemicals. Due to its unique structure, it can participate in a range of chemical reactions, including nucleophilic substitutions, addition reactions, and esterification. The compound is also known for its potential applications in the fragrance industry and as a component in the production of certain types of polymers.

3214-32-2

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3214-32-2 Usage

Physical state

Colorless liquid

Odor

Faint, pleasant

Uses

a. Solvent
b. Production of chemicals (pharmaceuticals, plastics, resins)
c. Flavoring agent in food
d. Fragrance in cosmetics

Flammability

Highly flammable

Safety precautions

Handle and store with care

Health hazards

a. Eye irritation
b. Skin irritation
c. Respiratory system irritation

Exposure concerns

High levels can cause health issues

Safety measures

Proper safety precautions should be taken when handling this substance

Check Digit Verification of cas no

The CAS Registry Mumber 3214-32-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,2,1 and 4 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3214-32:
(6*3)+(5*2)+(4*1)+(3*4)+(2*3)+(1*2)=52
52 % 10 = 2
So 3214-32-2 is a valid CAS Registry Number.

3214-32-2Relevant academic research and scientific papers

Intramolecular Addition of Alkoxy Radicals. Part 4. Reductive Cyclisation of Olefinic Hydroperoxides

Taillez, Bernard,Bertrand, Michele Paula,Surzur, Jean-Marie

, p. 547 - 554 (2007/10/02)

Pent-4-enyl hydroperoxide reacts with reducing salts (FeX2, TiCl3) to afford tetrahydrofurfuryl compounds (halides or dimers) in high yield from the selective cyclisation of the pent-4-enyloxy radical.Analogous behaviour is observed for photolysis although the yields of cyclic products are lower.The photolysis of hex-5-enyl hydroperoxide does not yield cyclic products but these are observed when this hydroperoxide is reduced by FeCl2.It is suggested that metallic salts are able to complex the alkoxyl radicals thereby making them more electrophilic and hence more prone to cyclise.

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