(2R,3R,4S,5R,6R)-2-(Acetoxymethyl)-6-(allyloxy)-tetrahydro-2H-pyran-3,4,5-triyl triacetate - Names and Identifiers
Name | ALLYL-TETRA-O-ACETYL-BETA-D-
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Synonyms | ALLYL-TETRA-O-ACETYL-BETA-D- allyl-tetra-o-acetyl-β-d-glucopyranoside Allyl2,3,4,6-tetra-O-acetyl-b-D-glucopyranoside Allyl-2,3,4,6-tetra-O-acetyl-β-D-glucopyranoside Allyl 2,3,4,6-teatra-O-acetyl-β-D-glucopyranoside acetic acid (3,4,5-triacetyloxy-6-prop-2-enoxy-2-oxanyl)methyl ester (2R,3R,4S,5R,6R)-2-(Acetoxymethyl)-6-(allyloxy)-tetrahydro-2H-pyran-3,4,5-triyl triacetate
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CAS | 10343-15-4
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EINECS | 1533716-785-6 |
(2R,3R,4S,5R,6R)-2-(Acetoxymethyl)-6-(allyloxy)-tetrahydro-2H-pyran-3,4,5-triyl triacetate - Physico-chemical Properties
Molecular Formula | C17H24O10
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Molar Mass | 388.37 |
Melting Point | 87-90°C(lit.) |
Storage Condition | Sealed in dry,2-8°C |
Physical and Chemical Properties | WGK Germany:3 |
(2R,3R,4S,5R,6R)-2-(Acetoxymethyl)-6-(allyloxy)-tetrahydro-2H-pyran-3,4,5-triyl triacetate - Risk and Safety
WGK Germany | 3 |
HS Code | 29400090 |
(2R,3R,4S,5R,6R)-2-(Acetoxymethyl)-6-(allyloxy)-tetrahydro-2H-pyran-3,4,5-triyl triacetate - Introduction
Allyl-tetra-O-acetyl-β-D-glucopyranoside is a compound whose chemical formula is C₂ H₂ O₂. The following is a description of the properties, uses, preparation and safety information of the compound:
Properties: Allyl-tetra-O-acetyl-β-D-glucopyranoside is a white or nearly white crystalline powder, insoluble in water, but soluble in organic solvents such as methanol and ethanol. It is a glycoside compound containing a pyran ring and a glucose unit. It is a common intermediate compound in chemical synthesis.
Application: Allyl-tetra-O-acetyl-β-D-glucopyranoside is widely used in organic synthesis. It can be used as a glycosyl reagent for the synthesis of biologically active natural products and drugs. In addition, it can also be used in the pharmaceutical field of drug research and development and manufacturing.
Preparation method: Allyl-tetra-O-acetyl-β-D-glucopyranoside was prepared by chemical synthesis. A common preparation method is to react a glycoside compound with an allyl group, followed by an acetic acid esterification reaction to obtain the target product.
Safety information: There are few studies on the toxicity and safety of allyl-tetra-O-acetyl-β-D-glucopyranoside, so it must be operated in the laboratory in accordance with relevant safety procedures. As with all chemicals, direct contact with skin and eyes should be avoided. In case of accidental contact, rinse immediately with plenty of water. At the same time, the compound should be stored and handled properly to avoid contact with flammable substances and oxidizing agents. To ensure safety, strictly follow the relevant safety procedures and recommendations.
Last Update:2024-04-09 21:11:58