What is the 4-BUTYROTHIOLACTONE?

4-BUTYROTHIOLACTONE is , while it's Molecular Formula is C4H6 O S. ?-Thiobutyrolactone was used to terminate the ring opening polymerization of ?-pentadecalactone to synthesize difunctional polyesters. ?-Thiobutyrolactone was used to study the mechanism of metabolism of sulphur containing heterocyclic compounds by lignin-degrading basidiomycete Coriolus versicolor.

What is the CAS number for 4-BUTYROTHIOLACTONE?

The CAS number of 4-BUTYROTHIOLACTONE is 1003-10-7.

What is 4-BUTYROTHIOLACTONE (1003-10-7) used for?

4-Butyrothiolactone, also known as ?-thiobutyrolactone, is a heterocyclic compound with a sulfur-containing ring structure. It is characterized by its ability to undergo copolymerization with other compounds, such as glycidyl phenyl ether, to form poly(ester-alt-sulfide). This unique property makes it a versatile compound with potential applications in various industries.InChI:InChI=1/C4H6OS/c5-4-2-1-3-6-4/h1-3H2

What is the 4-BUTYROTHIOLACTONE?

4-BUTYROTHIOLACTONE is , while it's Molecular Formula is C4H6 O S. γ-Thiobutyrolactone was used to terminate the ring opening polymerization of ω-pentadecalactone to synthesize difunctional polyesters. γ-Thiobutyrolactone was used to study the mechanism of metabolism of sulphur containing heterocyclic compounds by lignin-degrading basidiomycete Coriolus versicolor.

What is the CAS number for 4-BUTYROTHIOLACTONE?

The CAS number of 4-BUTYROTHIOLACTONE is 1003-10-7.

What is 4-BUTYROTHIOLACTONE (1003-10-7) used for?

4-Butyrothiolactone, also known as γ-thiobutyrolactone, is a heterocyclic compound with a sulfur-containing ring structure. It is characterized by its ability to undergo copolymerization with other compounds, such as glycidyl phenyl ether, to form poly(ester-alt-sulfide). This unique property makes it a versatile compound with potential applications in various industries.InChI:InChI=1/C4H6OS/c5-4-2-1-3-6-4/h1-3H2

Manufacturer Supply Best Quality 4-BUTYROTHIOLACTONE 1003-10-7 with Efficient Transportation

4-BUTYROTHIOLACTONE

CAS No.: 1003-10-7
Purity: 99%

Manufacturer Supply Best Quality 4-BUTYROTHIOLACTONE 1003-10-7 with Efficient Transportation

Molecular Formula: C4H6 O S
Molecular Weight: 102.157
Vapor Pressure: 0.38mmHg at 25°C
Melting Point: 138 °C(Solv: ethyl acetate (141-78-6))
Refractive Index: n20/D 1.523(lit.)
Boiling Point: 197.4°Cat760mmHg
Flash Point: 87.6°C
PSA： 42.37000
Density: 1.206g/cm³
LogP: 1.04000

4-BUTYROTHIOLACTONE(Cas 1003-10-7) Usage

General Description

γ-Thiobutyrolactone undergoes copolymerization with glycidyl phenyl ether to form poly(ester-alt-sulfide).

InChI:InChI=1/C4H6OS/c5-4-2-1-3-6-4/h1-3H2

1003-10-7 Relevant articles

N-NITROSAMINES AS REAGENTS FOR THE =C=S=C=O TRANSFORMATION

Jorgensen, K. A.,El-Wassimy, M. T. M.,Lawesson, S. -O.

, p. 469 - 474 (1983)

N-nitrosopiperidine and N-nitroso-N-meth...

AN EXCEPTIONALLY MILD, PHASE TRANSFER CATALYZED METHOD FOR THE CONVERSION OF THIOCARBONYL COMPOUNDS TO CARBONYLS

Alper, Howard,Kwiatkowska, Caroline,Petrignani, Jean-Francois,Sibtain, Fazle

, p. 5449 - 5450 (1986)

The thiocarbonyl group of thioketones, d...

-

Storm,D.R.,Koshland,D.E.

, p. 5815 - 5825 (1972)

Theoretical Study, Synthesis, and Reactivity of Five-Membered-Ring Acyl Sulfonium Cations

Rao, K.V. Raghavendra,Caiveau, Nicolas,David, Rolf,Shalayel, Ibrahim,Milet, Anne,Vallée, Yannick

, p. 6125 - 6129 (2015)

The feasibility of the cyclization of γ-...

Efficient Synthesis of γ-Lactones by Cobalt-Catalyzed Carbonylative Ring Expansion of Oxetanes under Syngas Atmosphere

Tang, Yitian,Shen, Chaoren,Yao, Qiyi,Tian, Xinxin,Wang, Bo,Dong, Kaiwu

, p. 5898 - 5902 (2020)

A practical route from oxetane or thieta...

Synthesis of thiolactones using benzyltriethylammonium tetrathiomolybdate as sulfur transfer reagent

Bhar, Debjani,Chandrasekaran

, p. 11835 - 11842 (1997)

An interesting sulfur transfer reaction ...

-

Hatada et al.

, p. 448,450 (1978)

Regiospecific Carbonylation and Ring Expansion of Thietanes and Oxetanes Catalyzed by Cobalt and/or Ruthenium Carbonyls

Wang, Ming-De,Calet, Serge,Alper, Howard

, p. 20 - 21 (1989)

Dicobalt octacarbonyl and triruthenium d...

Indium-catalyzed direct conversion of lactones into thiolactones using a disilathiane as a sulfur source

Ogiwara, Yohei,Takano, Ken,Horikawa, Shuhei,Sakai, Norio

, (2018/06/15)

An indium-catalyzed reaction of lactones...

COMPOUNDS FOR A CONTROLLED RELEASE OF ACTIVE PERFUMING MOLECULES

-

Page/Page column 39-40, (2013/10/08)

The present invention relates to the fie...

1003-10-7 Process route

: 96-48-0
4-butanolide

: 75-15-0,12122-00-8
carbon disulfide

: 1003-10-7
Thiobutyrolactone

Conditions

Conditions	Yield
With sodium sulfide; at 175 ℃;

: 96-48-0
4-butanolide

: 1003-10-7
Thiobutyrolactone

Conditions

Conditions	Yield
With aluminium oxide catalyst; hydrogen sulfide; at 350 ℃;
With indium(III) triflate; hexamethyldisilathiane; In 1,2-dichloro-benzene; at 80 ℃; for 24h; Sealed tube; Glovebox;	66 %Spectr.
With sodium sulfide; hydrogen sulfide; at 200 ℃;
With sodium sulfide; hydrogen sulfide; benzene; at 250 ℃;