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Phenyl 2-Deoxy-1-thio-2-(2,2,2-trichloroethoxyformamido)-beta-D-galactopyranoside is a complex chemical compound characterized by a phenyl group linked to a deoxythio galactopyranoside backbone, with an additional trichloroethoxyformamido group at the thio position on the galactopyranoside ring. Phenyl 2-Deoxy-1-thio-2-(2,2,2-trichloroethoxyformamido)-beta-D-galactopyranoside is distinguished by its unique structural features and is predominantly utilized in research environments.

868230-98-2

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868230-98-2 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, Phenyl 2-Deoxy-1-thio-2-(2,2,2-trichloroethoxyformamido)-beta-D-galactopyranoside 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.

Check Digit Verification of cas no

The CAS Registry Mumber 868230-98-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,8,2,3 and 0 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 868230-98:
(8*8)+(7*6)+(6*8)+(5*2)+(4*3)+(3*0)+(2*9)+(1*8)=202
202 % 10 = 2
So 868230-98-2 is a valid CAS Registry Number.
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

868230-98-2 Well-known Company Product Price

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  • TCI America

  • (P1643)  Phenyl 2-Deoxy-1-thio-2-(2,2,2-trichloroethoxyformamido)-β-D-galactopyranoside  

  • 868230-98-2

  • 0.00CNY

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868230-98-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2,2-trichloroethyl N-[(2S,3S,4R,5R,6S)-4,5-dihydroxy-6-(hydroxymethyl)-2-phenylsulfanyloxan-3-yl]carbamate

1.2 Other means of identification

Product number -
Other names Sodium Pelargonate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:868230-98-2 SDS

868230-98-2Relevant academic research and scientific papers

Synthesis and anti-inflammatory activity of gold-nanoparticle bearing a dermatan sulfate disaccharide analog

Shang, Chengxiang,Cai, Chao,Zhao, Cuixia,Du, Yuguo

supporting information, p. 81 - 83 (2017/09/08)

A dermatan sulfate (DS) repeating disaccharide analog, α-L-idopyranosiduronate-(1 → 3)-2-amino-2-deoxy-4,6-di-O-sulfo-β-D-galactopyranoside, has been convergently synthesized and successfully applied to prepare the GAG-functionalized gold glyconanoparticle. This new material exhibited good anti-inflammatory activity which was comparable to that of the drug ibuprofen incarrageenan-induced paw edema in a rat model.

First synthesis of C. difficile PS-II cell wall polysaccharide repeating unit

Danieli, Elisa,Lay, Luigi,Proietti, Daniela,Berti, Francesco,Costantino, Paolo,Adamo, Roberto

supporting information; experimental part, p. 378 - 381 (2011/04/15)

Clostridium difficile is the most commonly diagnosed cause of nosocomial diarrhea with increasing incidence and mortality among elderly and hospitalized patients. We report the first synthesis of the surface polysaccharide PS-II repeating unit and its non

Di-tert-butylsilylene-directed α-selective synthesis of 4-methylumbelliferyl T-antigen

Imamura, Akihiro,Ando, Hiromune,Ishida, Hideharu,Kiso, Makoto

, p. 4415 - 4418 (2007/10/03)

(Chemical Equation Presented) We have succeeded in the facile synthesis of 4-methylumbelliferyl T-antigen as a substrate for endo-α-N- acetylgalactosaminidase by exploiting the combination of the di-tert-butylsilylene effect and the Mitsunobu reaction.

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