γ-Thiobutyrolactone - CAS 1003-10-7

Catalog:	BB000169
Product Name:	γ-Thiobutyrolactone
CAS:	1003-10-7
Synonyms:	thiolan-2-one

Technical Data

Safety and Hazards

Patents

Literatures

Computed Properties

IUPAC Name:	thiolan-2-one
Description:	γ-Thiobutyrolactone (CAS# 1003-10-7) is a useful research chemical compound.
Molecular Weight:	102.15
Molecular Formula:	C4H6OS
Canonical SMILES:	C1CC(=O)SC1
InChI:	InChI=1S/C4H6OS/c5-4-2-1-3-6-4/h1-3H2
InChI Key:	KMSNYNIWEORQDJ-UHFFFAOYSA-N
Boiling Point:	197.4 °C at 760 mmHg
Density:	1.18 g/mL at 25 °C (lit.)
Appearance:	Clear colorless liquid
Storage:	Sealed in dry, Room Temperature
MDL:	MFCD00005479
LogP:	1.04000

Publication Number	Title	Priority Date
CN-112979968-A	Cartilage targeting zwitterionic polymer and preparation method and application thereof	20210416
CN-212396740-U	Preparation facilities of gamma-thiobutyrolactone	20200602
KR-20200037155-A	Sodium Secondary Battery having Graphite Felt as a Current Collector	20200320
KR-102125755-B1	Sodium Secondary Battery having Graphite Felt as a Current Collector	20200320
US-2021284778-A1	Photochromic polydiorganosiloxane vinylic crosslinkers	20200311

PMID	Publication Date	Title	Journal
22247228	20120701	Decreased paraoxonase 1 (PON1) lactonase activity in hemodialyzed and renal transplanted patients. A novel cardiovascular biomarker in end-stage renal disease	Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association
20483453	20100801	The use of superporous Ac-CGGASIKVAVS-OH-modified PHEMA scaffolds to promote cell adhesion and the differentiation of human fetal neural precursors	Biomaterials
19803523	20091106	An improved synthesis of the selective EP4 receptor agonist ONO-4819	The Journal of organic chemistry
19748147	20091101	Relations of lysophosphatidylcholine in low-density lipoprotein with serum lipoprotein-associated phospholipase A2, paraoxonase and homocysteine thiolactonase activities in patients with type 2 diabetes mellitus	Diabetes research and clinical practice
18688494	20080821	Synthesis of C60-fused tetrahydrothiophene derivatives via nucleophilic cycloaddition of thiocyanates	Organic & biomolecular chemistry

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Related Functional Groups

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[38401-73-9]
5-(3-Nitrophenyl)-2-thiophenecarbaldehyde
[179556-14-0]
Ethyl 5-(methylsulfonamido)-1H-indole-2-carboxylate
[610259-52-4]
Ethyl 1-(thiophen-2-ylsulfonyl)piperidine-3-carboxylate
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GHS Hazard Statement:	H302 (100%): Harmful if swallowed [Warning Acute toxicity, oral]
Precautionary Statement:	P264, P270, P301+P312, P330, and P501
Signal Word:	Warning

Complexity:	69.9
Compound Is Canonicalized:	Yes
Covalently-Bonded Unit Count:	1
Defined Atom Stereocenter Count:	0
Defined Bond Stereocenter Count:	0
Exact Mass:	102.01393598
Formal Charge:	0
Heavy Atom Count:	6
Hydrogen Bond Acceptor Count:	2
Hydrogen Bond Donor Count:	0
Isotope Atom Count:	0
Monoisotopic Mass:	102.01393598
Rotatable Bond Count:	0
Topological Polar Surface Area:	42.4 Å²
Undefined Atom Stereocenter Count:	0
Undefined Bond Stereocenter Count:	0
XLogP3:	0.7