D-arabino-Hex-1-enitol, 1,5-anhydro-2-deoxy-6-O-[tris(1-methylethyl)silyl]- - Names and Identifiers
Name | 6-O-(triisopropylsilyl)-D-glucal
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Synonyms | 6-O-(TRIISOPROPYLSILYL)-D-GLUCAL 6-O-(triisopropylsilyl)-D-glucal 6-O-(Triisopropylsilyl)-D-glucal 1,5-ANHYDRO-2-DEOXY-6-O-(TRIISOPROPYLSILYL)-D-ARABINO-HEX-1-ENITOL (2R,3S,4R)-2-[tri(propan-2-yl)silyloxymethyl]-3,4-dihydro-2H-pyran-3,4-diol (2R,3S,4R)-2-(((Triisopropylsilyl)oxy)methyl)-3,4-dihydro-2H-pyran-3,4-diol D-arabino-Hex-1-enitol, 1,5-anhydro-2-deoxy-6-O-[tris(1-methylethyl)silyl]-
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CAS | 137915-37-8
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InChI | InChI=1/C15H30O4Si/c1-10(2)20(11(3)4,12(5)6)19-9-14-15(17)13(16)7-8-18-14/h7-8,10-17H,9H2,1-6H3/t13-,14-,15+/m1/s1 |
D-arabino-Hex-1-enitol, 1,5-anhydro-2-deoxy-6-O-[tris(1-methylethyl)silyl]- - Physico-chemical Properties
Molecular Formula | C15H30O4Si
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Molar Mass | 302.48 |
Density | 0.726g/mLat 25°C(lit.) |
Boling Point | 361.886°C at 760 mmHg |
Flash Point | 113°C |
Vapor Presure | 0mmHg at 25°C |
Storage Condition | Room Temprature |
Refractive Index | n20/D 1.489(lit.) |
D-arabino-Hex-1-enitol, 1,5-anhydro-2-deoxy-6-O-[tris(1-methylethyl)silyl]- - Risk and Safety
D-arabino-Hex-1-enitol, 1,5-anhydro-2-deoxy-6-O-[tris(1-methylethyl)silyl]- - Introduction
6-O-(triisopropylsilyl)-D-glucose is an organosilicon compound with the following properties:
1. Appearance features: colorless or light yellow solid.
2. solubility: soluble in organic solvents, insoluble in water.
3. melting point: about 100-110 degrees Celsius.
4. Stability: It is relatively stable at room temperature, but it will decompose under high temperature and strong acid and alkali conditions.
The main uses of this compound are as follows:
1. cosmetics: commonly used in skin care products and cosmetics, with the role of adjusting gloss and increase the smoothness of the touch.
2. pharmaceutical field: can be used for the modification of drug carriers to improve the solubility and bioavailability of drugs.
3. dyes and pigments: can be used as organic dyes and pigments synthesis intermediates.
On the preparation method, a common synthesis method is to react 3,4,6-three-position protected glucose with isopropylchlorosilane, and then remove the protecting group to obtain the target product.
In terms of safety information, this compound is an organosilicon compound and is generally considered to be relatively safe under normal operating conditions. However, the specific safety and protection requirements need to be determined according to the specific experimental conditions, in order to avoid unnecessary exposure and potential risks.
Last Update:2024-04-09 21:48:26