(S)-(+)-Epichlorohydrin CAS No. 67843-74-7
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Category：Pharmaceutical Materials Own Brand：MT /MOQ:100KG /From China/ B2B only.
Introduction
As a potential metabolic regulator, it is used to synthesize fatty acid oxidation inhibitors, for the total synthesis of Macquarimicins and the synthesis of macrolides RK-397, and for the synthesis of chiral intermediates and chiral drugs.
Product Name
(S)-(+)-Epichlorohydrin
(S) Multiple Names
-(+)-Epichlorohydrin;
(S)-(+)Epichlorohydrin;
(S)-Epichlorohydrin;
(2S)-2-(Chloromethyl)Oxirane
CAS No. 67843-74-7
EC No. 614-150-5
MF No. C3H5ClO
MW No. 92.5242
Advantage of (S)-(+)-Epichlorohydrin CAS No. 67843-74-7
Chiral structural units for enantioselective synthesis of hydroxyisoxazolidine and (+) – cis-sylvaticin (a potential antitumor agent)
Widely used in chemical filed
Easy to stock
| Aspect | Details |
|---|---|
| Product Name | (S)-(+)-Epichlorohydrin |
| Chemical Name | (S)-(+)-1-Chloro-2.3-epoxypropane |
| CAS Number | 67843-74-7 |
| Chemical Formula | C₃H₅ClO |
| Molecular Weight | 92.52 g/mol |
| Physical State | Colorless to very pale yellow liquid |
| Physical Properties | – Melting Point: -57°C – Boiling Point: 92–93°C at 360 mmHg – Density: 1.183 g/mL at 25°C – Refractive Index: 1.438 at 20°C – Flash Point: 93°F (33.9°C) – Solubility: Insoluble in water, soluble in chloroform and methanol |
| Reactivity | Highly reactive due to the presence of the epoxide ring, which can undergo ring-opening reactions with nucleophiles such as water, alcohols, and amines. |
| Main Uses | – Organic Synthesis: Used as a chiral intermediate in the synthesis of pharmaceuticals and agrochemicals. – Polymer Chemistry: Employed in the production of epoxy resins and polymers. – Biochemistry: Utilized in the synthesis of chiral molecules and bioactive compounds. |
| Packaging | Typically available in 1 kg, 5 kg, 25 kg, or 230 kg drums |
| Storage Conditions | Stored in a cool, dry, and well-ventilated area, away from heat, light, and moisture |
| Safety Precautions | Flammable liquid and vapor; toxic by inhalation, skin contact, and ingestion; causes severe skin burns and eye damage |
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