(S)-3-Acetoxy-gamma-butyrolactone

Base Information

Chemical Name:(S)-3-Acetoxy-gamma-butyrolactone
CAS No.:191403-65-3
Molecular Formula:C₆H₈O₄
Molecular Weight:144.127
Hs Code.:
DSSTox Substance ID:DTXSID60370074
Wikidata:Q82157390
Mol file:191403-65-3.mol

Synonyms:(S)-3-Acetoxy-gamma-butyrolactone;191403-65-3;[(3S)-5-oxooxolan-3-yl] acetate;(S)-5-Oxotetrahydrofuran-3-yl acetate;SCHEMBL4917217;DTXSID60370074;(s)-beta-acetoxy-gamma-butyrolactone;(R,S)-5-oxo-tetrahydrofuran-3-yl acetate;2(3H)-Furanone,4-(acetyloxy)dihydro-,(4S)-;A813488;tert-butyl ((3R,4R)-1-benzyl-3-methylpiperidin-4-yl)carbamate

Suppliers and Price of (S)-3-Acetoxy-gamma-butyrolactone

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

American Custom Chemicals Corporation
(S)-3-ACETOXY-GAMMA-BUTYROLACTONE 95.00%
5MG
$ 495.59

AHH
(S)-3-Acetoxy-gamma-butyrolactone 95%
5g
$ 280.00

Total 11 raw suppliers

Chemical Property of (S)-3-Acetoxy-gamma-butyrolactone

Chemical Property:

Appearance/Colour:clear yellow liquid
Vapor Pressure:0.00882mmHg at 25°C
Refractive Index:1.448-1.452
Boiling Point:266.1 °C at 760 mmHg
Flash Point:138.5 °C
PSA：52.60000
Density:1.23 g/cm³
LogP:-0.13500
XLogP3:-0.2
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:2
Exact Mass:144.04225873
Heavy Atom Count:10
Complexity:163

Purity/Quality:

97% ^*data from raw suppliers

(S)-3-ACETOXY-GAMMA-BUTYROLACTONE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s): Xi
Hazard Codes:Xi
Statements: 36/37/38
Safety Statements: 37/39-26

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(=O)OC1CC(=O)OC1
Isomeric SMILES:CC(=O)O[C@H]1CC(=O)OC1

Technology Process of (S)-3-Acetoxy-gamma-butyrolactone

There total 4 articles about (S)-3-Acetoxy-gamma-butyrolactone which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 85.0%

: 59025-03-5
(S)-acetoxysuccinic anhydride

: 191403-65-3
(3S)-β-acetoxy-γ-butyrolactone

Guidance literature:: (S)-acetoxysuccinic anhydride; With zinc(II) tetrahydroborate; In tetrahydrofuran; at 5 - 20 ℃; for 4h;

With hydrogenchloride; In water; at 5 ℃; for 0.5h;