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1-(α-tetrahydrofuryl)pentan-3-ol is a complex organic compound with the molecular formula C10H20O2. It is a secondary alcohol, characterized by the presence of a hydroxyl group (-OH) attached to a carbon atom in the pentan-3-ol chain. The α-tetrahydrofuryl group is a cyclic ether derived from tetrahydrofuran, which is attached to the first carbon of the pentan-3-ol chain. 1-(α-tetrahydrofuryl)pentan-3-ol is known for its unique chemical structure and potential applications in various fields, such as pharmaceuticals and chemical synthesis. Due to its specific functional groups and cyclic structure, it exhibits distinct chemical properties and reactivity, making it an interesting subject for research and development in the field of organic chemistry.

4469-83-4

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4469-83-4 Usage

Physical state

Colorless liquid

Odor

Faint, sweet

Toxicity

Relatively non-toxic

Irritation

Non-irritating to skin and eyes

Derivation

Furfuryl alcohol and pentan-3-ol

Applications

a. Solvent in chemical reactions and processes
b. Production of pharmaceuticals
c. Production of agrochemicals
d. Industrial applications

Uses

a. Solvent in resin production
b. Solvent in coating production
c. Solvent in adhesive production

Safety features

a. Low volatility
b. Low flammability

Environmental considerations

Preferred choice for industrial processes due to safety and environmental concerns

Check Digit Verification of cas no

The CAS Registry Mumber 4469-83-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,6 and 9 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 4469-83:
(6*4)+(5*4)+(4*6)+(3*9)+(2*8)+(1*3)=114
114 % 10 = 4
So 4469-83-4 is a valid CAS Registry Number.

4469-83-4Relevant academic research and scientific papers

Exo and endohormones. XX. Synthesis of racemic 2-ethyl-1,6-dioxaspiro[4,4]nonane, the aggregation pheromone of pityogenes chalcographus (Coleoptera, Scolytidae)

Balea, Ana,Pojar-fene?an, Maria,Pop, Lidia,Oprean, Ioan,Ciupe, Hilke

, p. 465 - 469 (2007/10/03)

The synthesis of a diastereoisomeric mixture of 2-etyl-1,6-dioxaspiro[4,4]nonane (chalcograne) a main component of the aggregation pheromone of the spruce bark beetle Pityogenes chalcographus (Coleoptera, Scolytidae), a serious pest in European forests, by 1,7-nonanediol cyclization using Pb(OAc)4 is given below. The side products of spirocyclization were identified by GC/MS.

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