1-硫-乙基-2,3,4-三-氧-苄基-B-L-硫代呋喃岩藻糖苷

1-硫-乙基-2,3,4-三-氧-苄基-B-L-硫代呋喃岩藻糖苷 - Names and Identifiers

Name	2,3,4-TRI-O-BENZYL-1-S-ETHYL-BETA-L-THIOFUCOPYRANOSIDE
Synonyms	2,3,4-TRI-O-BENZYL-1-S-ETHYL-BETA-L-THIO Ethyl 2,3,4-tri-O-benzyl-b-L-thiofucopyranoside Ethyl 2,3,4,-tri-O-benzyl-L-thiofucosepyranosid 2,3,4-Tri-O-benzyl-1-S-ethyl-L-thiofucopyranoside 2,3,4-tri-o-benzyl-1-s-ethyl-β-l-thiofucopyranoside ETHYL 2,3,4-TRI-O-BENZYL-1-THIO-BETA-L-FUCOPYRANOSIDE 2,3,4-TRI-O-BENZYL-1-S-ETHYL-BETA-L-THIOFUCOPYRANOSIDE ethyl 2,3,4-tri-O-benzyl-6-deoxy-1-thio-beta-L-galactopyranoside b-L-Galactopyranoside, ethyl6-deoxy-2,3,4-tris-O-(phenylmethyl)-1-thio- b-L-Galactopyranoside, ethyl 6-deoxy-2,3,4-tris-O-(phenylMethyl)-1-thio-
CAS	116391-11-8 99409-34-4
InChI	InChI=1/C29H34O4S/c1-3-34-29-28(32-21-25-17-11-6-12-18-25)27(31-20-24-15-9-5-10-16-24)26(22(2)33-29)30-19-23-13-7-4-8-14-23/h4-18,22,26-29H,3,19-21H2,1-2H3/t22-,26+,27+,28-,29+/m0/s1

1-硫-乙基-2,3,4-三-氧-苄基-B-L-硫代呋喃岩藻糖苷 - Physico-chemical Properties

Molecular Formula	C29H34O4S
Molar Mass	478.65
Density	1.16g/cm³
Melting Point	52-54°C(lit.)
Boling Point	592.1°C at 760 mmHg
Flash Point	>230°F
Vapor Presure	2.27E-13mmHg at 25°C
Refractive Index	1.596
Physical and Chemical Properties	WGK Germany:3

1-硫-乙基-2,3,4-三-氧-苄基-B-L-硫代呋喃岩藻糖苷 - Risk and Safety

WGK Germany

1-硫-乙基-2,3,4-三-氧-苄基-B-L-硫代呋喃岩藻糖苷 - Introduction

1-Thio-ethyl-2, 3,4-tri-oxo-benzyl-b-L-thiofuranofucosides is an organic compound often abbreviated as STOG with the chemical formula C16H22O9S.

The compound has the following properties:
1. Appearance: STOG is white or white solid.
2. Solubility: STOG is soluble in water and other solvents, such as methanol and acetonitrile.
3. Hydrolysis: STOG is easily hydrolyzed by enzymes.

Main uses of STOG:
1. Biological research: STOG is commonly used to study the metabolism and signal transduction mechanism of carbohydrates in vivo.
2. Drug development: STOG can be used as a carrier or additive for the design and development of drug delivery systems.

Method of preparing STOG:
The synthesis of STOG is usually carried out by a chemical synthesis method. Sulfur and ethyl groups can be introduced, for example, by benzylation and thiolenylation reactions, followed by further oxapol (Oxathiazepin) ring formation.

Safety Information:
1. STOG has not been evaluated as a toxic substance, but should follow laboratory safety procedures when used.
2. Avoid contact with skin and eyes. If contact occurs, rinse immediately with plenty of water.
3. in storage and handling, should avoid high temperature and fire.

Please note that for specific chemical substances, it is important to understand and follow the relevant safety guidelines.

Last Update：2024-04-09 15:17:51