What is the 3-Buten-2-ol?

3-Buten-2-ol is clear colorless liquid, while it's Molecular Formula is C4H8O. clear colorless liquid 3-Buten-2-ol is a useful compound in organic synthesis.

What is the CAS number for 3-Buten-2-ol?

The CAS number of 3-Buten-2-ol is 598-32-3.

What is 3-Buten-2-ol (598-32-3) used for?

3-Buten-2-ol (also known as methylvinylcarbinol) is an unsaturated alcohol that can form acetals, which undergo hydrolysis without allylic rearrangement, as demonstrated in the study. The hydrolysis of its acetal derivative proceeds via a normal pathway, yielding the original alcohol without forming carbonium ion intermediates or undergoing abnormal cleavage, highlighting its stability under these conditions. This behavior contrasts with other carbinols, such as phenylvinylcarbinol, which may isomerize during hydrolysis. The study underscores the preference for direct hydrolysis in 3-buten-2-ol derivatives, preserving their structure.InChI:InChI=1/C4H8O/c1-3-4(2)5/h3-5H,1H2,2H3/t4-/m0/s1

What is the 3-Buten-2-ol?

3-Buten-2-ol is clear colorless liquid, while it's Molecular Formula is C4H8O. clear colorless liquid 3-Buten-2-ol is a useful compound in organic synthesis.

What is the CAS number for 3-Buten-2-ol?

The CAS number of 3-Buten-2-ol is 598-32-3.

What is 3-Buten-2-ol (598-32-3) used for?

3-Buten-2-ol (also known as methylvinylcarbinol) is an unsaturated alcohol that can form acetals, which undergo hydrolysis without allylic rearrangement, as demonstrated in the study. The hydrolysis of its acetal derivative proceeds via a normal pathway, yielding the original alcohol without forming carbonium ion intermediates or undergoing abnormal cleavage, highlighting its stability under these conditions. This behavior contrasts with other carbinols, such as phenylvinylcarbinol, which may isomerize during hydrolysis. The study underscores the preference for direct hydrolysis in 3-buten-2-ol derivatives, preserving their structure.InChI:InChI=1/C4H8O/c1-3-4(2)5/h3-5H,1H2,2H3/t4-/m0/s1

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Product classification

3-Buten-2-ol

Name: 3-Buten-2-ol
CAS: 598-32-3
Purity: 99%

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Details

3-Buten-2-ol 598-32-3 with purity >99% Low price in stock

Molecular Formula: C4H8O
Molecular Weight: 72.1069
Appearance/Colour: clear colorless liquid
Vapor Pressure: 24.4mmHg at 25°C
Melting Point: -100 °C
Refractive Index: n20/D 1.415(lit.)
Boiling Point: 97.3 °C at 760 mmHg
PKA: 14.49±0.20(Predicted)
Flash Point: 16.7 °C
PSA： 20.23000
Density: 0.823 g/cm³
LogP: 0.55320

3-Buten-2-ol(Cas 598-32-3) Usage

General Description	3-Buten-2-ol is a flavor and fragrance standard provided by Sigma-Aldrich?. Flavors and fragrances are widely used to add taste and/or smell to products without aroma, to mask unpleasant odors and to maintain stability of original flavor.
Hazard	50 ppm for 15 minutes causes eye irritation; A skin and strong eye irritant;
storage	Store in cool. Keep container tightly closed in a dry and well-ventilated place. Store away from oxidizing agent.

InChI:InChI=1/C4H8O/c1-3-4(2)5/h3-5H,1H2,2H3/t4-/m0/s1

598-32-3 Relevant articles

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Fuchs,Van-derWerf

, p. 5917 (1952)

Asymmetric Catalysis by Vitamin B12. The isomerization of Achiral Epoxides to Optically Active Allylic Alcohols

Su, Heng,Walder, Lorenz,Zhang, Zhong-da,Scheffold, Rolf

, p. 1073 - 1078 (1988)

Achiral epoxides are isomerized to optic...

Evidence for a Concerted SN2' Mechanism in the Gas-Phase Acid-induced Nucleophilic Substitutions on Allylic Substrates

Dezi, Emanuela,Lombardozzi, Antonietta,Pizzabiocca, Adriano,Renzi, Gabriele,Speranza, Maurizio

, p. 547 - 548 (1995)

Gas phase nucleophilic substitution on o...

Active site structure of a lithium phosphate catalyst for the isomerization of 2,3-epoxybutane to 3-buten-2-ol

Kim, Tae Yong,Song, Chyan Kyung,Yun, Yang Sik,Yun, Danim,Han, Jeong Woo,Yi, Jongheop

, p. 133 - 141 (2018)

Basic lithium phosphate (B-LPO) catalyst...

THE cis REDUCTION OF 4-(TRIMETHYLSILYL)-3-BUTYN-2-OL WITH LITHIUM ALUMINIUM HYDRIDE

Mancini, Michael L.,Honek, John F.

, p. 4295 - 4298 (1983)

A systematic study led to a method for t...

Probing Molecular Motion and Chemical Reactions inside the Chiral Tri-o-thymotide Clathrate Cavity by Solid State NMR Techniques

Facey, Glenn,Ripmeester, John A.

, p. 1585 - 1587 (1990)

Solid state NMR techniques offer a non-d...

Dehydration of 2,3-butanediol to produce 1,3-butadiene over Sc2O3 catalyst prepared through hydrothermal aging

Nakazono, Kazuki,Sato, Satoshi,Takahashi, Ryoji,Yamada, Yasuhiro

, (2021/11/16)

Vapor-phase catalytic dehydration of 2,3...

Selective production of 1,3-butadiene from 1,3-butanediol over Y2Zr2O7 catalyst

Matsuda, Asami,Matsumura, Yoshitaka,Sato, Satoshi,Yamada, Yasuhiro

, p. 1651 - 1658 (2021/07/21)

The vapor-phase dehydration of 1,3-butan...

Regio- And Enantioselective Iridium-Catalyzed Amination of Alkyl-Substituted Allylic Acetates with Secondary Amines

Jung, Woo-Ok,Krische, Michael J.,Migliozzi, Madyson M.,Stivala, Craig E.,Yoo, Minjin,Zbieg, Jason R.

supporting information, (2021/12/27)

Robust air-stable cyclometalated π-allyl...

PROCESS FOR PRODUCING DIENES

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Page/Page column 30-34, (2021/06/26)

A process for producing a diene, prefera...

598-32-3 Process route

: 4784-77-4,29576-14-5,39616-19-8
(E/Z)-crotyl bromide

: 598-32-3
2-hydroxy-3-butene

: 6117-91-5,542-72-3
(E/Z)-2-buten-1-ol

Conditions

Conditions	Yield
With sodium carbonate;
With potassium carbonate;
With sodium carbonate;

: 563-52-0,35729-37-4
2-chloro-3-butene

: 598-32-3
2-hydroxy-3-butene

: 6117-91-5,542-72-3
(E/Z)-2-buten-1-ol