868230-98-2

Basic information

• Product Name: Phenyl 2-Deoxy-1-thio-2-(2,2,2-trichloroethoxyformamido)-beta-D-galactopyranoside
• Synonyms: Phenyl 2-Deoxy-1-thio-2-(2,2,2-trichloroethoxyformamido)-beta-D-galactopyranoside;Phenyl 2-Deoxy-1-thio-2-(2,2,2-trichloroethoxyforMaMido)-β-D-galactopyranoside
• CAS NO: 868230-98-2
• Molecular Formula: C₁₅H₁₈Cl₃NO₆S
• Molecular Weight: 446.733
• Mol File: 868230-98-2.mol

Chemical Properties

• Boiling Point: 628.852°C at 760 mmHg
• Flash Point: 334.118°C
• Appearance: /
• Density: 1.598g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.639
• CAS DataBase Reference: Phenyl 2-Deoxy-1-thio-2-(2,2,2-trichloroethoxyformamido)-beta-D-galactopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: Phenyl 2-Deoxy-1-thio-2-(2,2,2-trichloroethoxyformamido)-beta-D-galactopyranoside(868230-98-2)
• EPA Substance Registry System: Phenyl 2-Deoxy-1-thio-2-(2,2,2-trichloroethoxyformamido)-beta-D-galactopyranoside(868230-98-2)

Safety Data

• Hazardous Substances Data: 868230-98-2(Hazardous Substances Data)

Usage

Uses

Used in Research Applications:
Phenyl 2-Deoxy-1-thio-2-(2,2,2-trichloroethoxyformamido)-beta-D-galactopyranoside serves as a glycosyltransferase inhibitor, which is instrumental in halting the enzymatic processes that lead to glycosylation. This makes it a crucial tool in the study of carbohydrate processing and cell signaling mechanisms.
Used in Pharmaceutical Research:
In the pharmaceutical industry, this compound is used as a research tool for drug discovery, particularly in the development of new therapeutic agents targeting glycosylation pathways, which are implicated in various diseases.
Used in Carbohydrate Processing Studies:
Phenyl 2-Deoxy-1-thio-2-(2,2,2-trichloroethoxyformamido)-beta-D-galactopyranoside is applied in the investigation of biological processes that involve glycosidic bonds and carbohydrate molecules, providing insights into their role in cellular functions and interactions.
Used in Cell Signaling Research:
Phenyl 2-Deoxy-1-thio-2-(2,2,2-trichloroethoxyformamido)-beta-D-galactopyranoside is also valuable in research focused on cell signaling, where glycosylation plays a critical role in modulating cellular communication and response to stimuli.
Overall, Phenyl 2-Deoxy-1-thio-2-(2,2,2-trichloroethoxyformamido)-beta-D-galactopyranoside is a specialized chemical with a niche but significant role in advancing scientific understanding and potentially contributing to the development of new medical treatments.

InChI:InChI=1/C15H18Cl3NO6S/c16-15(17,18)7-24-14(23)19-10-12(22)11(21)9(6-20)25-13(10)26-8-4-2-1-3-5-8/h1-5,9-13,20-22H,6-7H2,(H,19,23)/t9-,10-,11-,12+,13-/m0/s1

Upstream product

• 278784-83-1 phenyl 3,4,6-tri-O-acetyl-2-deoxy-1-thio-2-(2',2',2'-trichloroethoxycarbonylamino)-β-D-galactopyranoside 

Downstream Products

• 612844-08-3 phenyl 2-deoxy-4,6-O-di-tert-butylsilylene-3-O-(2,2,2-trichloroethoxycarbonyl)-2-(2,2,2-trichloroethoxycarbonylamino)-1-thio-β-D-galactopyranoside 
• 868230-99-3 phenyl 2-deoxy-4,6-O-di-tert-butylsilylene-1-thio-2-(2,2,2-trichloroethoxycarbonylamino)-β-D-galactopyranoside 
• 920537-10-6 C₆₅H₈₁Cl₃N₂O₂₆SSi 
• 612844-16-3 phenyl 2-acetamido-3-O-acetyl-2-deoxy-4,6-O-di-tert-butylsilylene-β-D-galactopyranoside 
• 612844-13-0 Acetic acid (4aR,6S,7R,8R,8aR)-2,2-di-tert-butyl-6-phenylsulfanyl-7-(2,2,2-trichloro-ethoxycarbonylamino)-hexahydro-1,3,5-trioxa-2-sila-naphthalen-8-yl ester 
• 868231-01-0 phenyl 2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl-(1->3)-2-deoxy-4,6-O-di-tert-butylsilylene-1-thio-2-(2,2,2-trichloroethoxycarbonylamino)-β-D-galactopyranoside 
• 1262208-49-0 phenylthio 2-O-acetyl-3,4,6-tri-O-benzyl-β-D-glucopyranosyl-(1->3)-4,6-O-benzylidene-2-deoxy-2-(2',2',2'-trichloroethoxycarbonylamino)-β-D-galactopyranoside 
• 1262208-53-6 phenylthio 2-O-acetyl-3,4-di-O-benzyl-6-O-tert-butyldiphenylsilyl-β-D-glucopyranosyl-(1->3)-4,6-O-benzylidene-2-deoxy-2-(2',2',2'-trichloroethoxycarbonylamino)-β-D-galactopyranoside 

Relevant articles and documents

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