NSC 404076 - Names and Identifiers
Name | (2S,4S,5R)-2-allyloxy-6-(hydroxymethyl)tetrahydropyran-3,4,5-triol
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Synonyms | NSC 404076 Ally a-D-galactopyranoside Allyl-α-D-galactopyranoside ALLYL A-D-GALACTOPYRANOSIDE allyl α-d-galactopyranoside α-D-Glucose Monoallyl Ether ALLYL ALPHA-D-GALACTOPYRANOSIDE (2S,4S,5R)-2-allyloxy-6-(hydroxymethyl)tetrahydropyran-3,4,5-triol
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CAS | 48149-72-0
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EINECS | 1533716-785-6 |
InChI | InChI=1/C9H16O6/c1-2-3-14-9-8(13)7(12)6(11)5(4-10)15-9/h2,5-13H,1,3-4H2/t5?,6-,7-,8?,9-/m0/s1 |
InChIKey | XJNKZTHFPGIJNS-NXRLNHOXSA-N |
NSC 404076 - Physico-chemical Properties
Molecular Formula | C9H16O6
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Molar Mass | 220.22 |
Density | 1.37±0.1 g/cm3(Predicted) |
Melting Point | 141-145°C(lit.) |
Boling Point | 415.0±45.0 °C(Predicted) |
Flash Point | 204.808°C |
Solubility | Methanol (Slightly), Water (Slightly) |
Vapor Presure | 0mmHg at 25°C |
Appearance | Solid |
Color | White to Off-White |
pKa | 13.01±0.70(Predicted) |
Storage Condition | 2-8°C |
Refractive Index | 1.55 |
NSC 404076 - Risk and Safety
WGK Germany | 3 |
HS Code | 29400090 |
NSC 404076 - Introduction
(2S,4S,5R)-2-allyloxy-6-(hydroxymethyl)tetrahydropyran-3,4,5-triol is an organic compound with the chemical structure shown below:((2S,4S,5R)-2-allyloxy-6-(hydroxymethyl)tetrahydropyran-3,4,5-triol).
Nature:
(2S,4S,5R)-2-allyloxy-6-(hydroxymethyl)tetrahydropyran-3 is a white crystalline solid, soluble in water. It is a glycoside compound consisting of a pyranyl ring and a galactose structure. It has a visible bi-photoelectric effect and can be used as a chiral initiator in chemical reactions.
Use:
(2S,4S,5R)-2-allyloxy-6-(hydroxymethyl)tetrahydropyran-3,4,5-triol are widely used in organic synthesis. It can be used to catalyze epoxidation reactions, condensation reactions and ketone reduction reactions, etc. In addition, it can also serve as a substrate or transition state in drug synthesis.
Preparation Method:
The preparation of (2S,4S,5R)-2-allyloxy-6-(hydroxymethyl)tetrahydropyran-3,4,5-triol is usually carried out by glycosidation reaction. A common method is the reaction of α-D-pyranose with allyl alcohol under acidic conditions to give (2S,4S,5R)-2-allyloxy-6-(hydroxymethyl)tetrahydropyran-3,4,5-triol. The method has good yield and selectivity.
Safety Information:
(2S,4S,5R)-2-allyloxy-6-(hydroxymethyl)tetrahydropyran-3,4,5-triol is generally considered relatively safe, but it is still recommended to wear personal protective equipment, such as gloves, glasses and laboratory coats. Relevant safety regulations and operating procedures shall be observed during storage and disposal. In case of ingestion, inhalation or direct contact, seek medical help immediately.
Last Update:2024-04-09 15:17:58