L-Gulonolactone acetonide, 2,3-O-Isopropylidene-L-gulonic acid, gamma-lactone - Names and Identifiers
Name | 2,3-O-Isopropylidene-L-gulonolactone
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Synonyms | 2,3-O-Isopropylidene-L-gulonolactone 2,3-O-Isopropylidene-L-gulono-1,4-lactone 2,3-O-Isopropylidene-L-gulonic acid-1,4-lactone 2,3-O-(1-Methylethylidene)-L-gulonic Acid γ-Lactone L-Gulonic acid, 2,3-O-(1-methylethylidene)-, γ-lactone L-Gulonolactone acetonide, 2,3-O-Isopropylidene-L-gulonic acid, gamma-lactone
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CAS | 94840-08-1
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L-Gulonolactone acetonide, 2,3-O-Isopropylidene-L-gulonic acid, gamma-lactone - Physico-chemical Properties
Molecular Formula | C9H14O6
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Molar Mass | 218.2 |
Storage Condition | 2-8℃ |
L-Gulonolactone acetonide, 2,3-O-Isopropylidene-L-gulonic acid, gamma-lactone - Upstream Downstream Industry
L-Gulonolactone acetonide, 2,3-O-Isopropylidene-L-gulonic acid, gamma-lactone - Introduction
2, is an organic compound with the chemical formula C8H12O5. It is a white crystalline solid, soluble in water and some organic solvents.
This compound has certain uses in the field of biochemistry. It is an important intermediate commonly used in the synthesis of vitamin C (ascorbic acid). It can also be used as a starting material for pharmaceutical chemical synthesis and natural product synthesis.
2, the preparation method of acetal is usually by reacting 5-hydroxymethylfurfural with isopropanol, and performing an acetal reaction under acidic conditions to produce the desired product.
Regarding safety information, this compound is usually relatively safe when used and handled correctly. However, it can be irritating to the eyes, skin and respiratory system. Avoid direct contact with skin and eyes, and take appropriate protective measures during operation, such as wearing gloves and safety glasses. During processing and storage, please follow the corresponding safety operation guidelines to ensure the safety of personnel and the environment.
Last Update:2024-04-09 20:45:29