Welcome to LookChem.com Sign In|Join Free
  • or
4-Methylumbelliferyl 2-Azido-2-deoxy-4,6-O-phenylMethylene-α-D-galactopyranoside is a complex organic compound with a unique chemical structure. It is a colorless solid that is characterized by its distinct functional groups, including an azido group, a deoxy sugar moiety, and a phenylmethylene bridge. 4-MethyluMbelliferyl 2-Azido-2-deoxy-4,6-O-phenylMethylene-α-D-galactopyranoside is known for its potential applications in various fields due to its unique properties and reactivity.

1147438-59-2

Post Buying Request

1147438-59-2 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

1147438-59-2 Usage

Uses

Used in Synthesis:
4-Methylumbelliferyl 2-Azido-2-deoxy-4,6-O-phenylMethylene-α-D-galactopyranoside is used as a synthetic intermediate for the preparation of 4-Methylumbelliferyl α-T-antigen. This application is based on its ability to serve as a key building block in the synthesis of complex carbohydrates and glycoconjugates, which are important in various biological processes and have potential applications in the development of new drugs and diagnostic tools.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 4-Methylumbelliferyl 2-Azido-2-deoxy-4,6-O-phenylMethylene-α-D-galactopyranoside is used as a precursor in the synthesis of various therapeutic agents. Its unique structure allows for the development of novel compounds with potential applications in the treatment of various diseases, including cancer and infectious diseases.
Used in Research and Development:
4-Methylumbelliferyl 2-Azido-2-deoxy-4,6-O-phenylMethylene-α-D-galactopyranoside is also used in research and development for the study of carbohydrate chemistry, glycobiology, and related fields. Its unique structure and reactivity make it a valuable tool for understanding the role of carbohydrates in biological systems and for the development of new methods and techniques in these areas.
Used in Diagnostic Applications:
Due to its fluorescent properties, 4-Methylumbelliferyl 2-Azido-2-deoxy-4,6-O-phenylMethylene-α-D-galactopyranoside can be used in the development of diagnostic assays and tests. Its ability to be detected through fluorescence can be exploited in the design of sensitive and specific assays for the detection of various biological targets, including enzymes, receptors, and other molecules of interest.

Check Digit Verification of cas no

The CAS Registry Mumber 1147438-59-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,4,7,4,3 and 8 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1147438-59:
(9*1)+(8*1)+(7*4)+(6*7)+(5*4)+(4*3)+(3*8)+(2*5)+(1*9)=162
162 % 10 = 2
So 1147438-59-2 is a valid CAS Registry Number.

1147438-59-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-[[(2S,4aR,6R,7R,8R,8aR)-7-azido-8-hydroxy-2-phenyl-4,4a,6,7,8,8a-hexahydropyrano[3,2-d][1,3]dioxin-6-yl]oxy]-4-methylchromen-2-one

1.2 Other means of identification

Product number -
Other names 4-Methylumbelliferyl 2-Azido-2-deoxy-4,6-O-phenylmethylene-|A-D-galactopyranoside

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:1147438-59-2 SDS

1147438-59-2Upstream product

1147438-59-2Relevant academic research and scientific papers

A straightforward α-selective aromatic glycosylation and its application for stereospecific synthesis of 4-methylumbelliferyl α-T-antigen

Chang, Shih-Sheng,Lin, Chun-Cheng,Li, Yaw-Kuen,Mong, Kwok-Kong Tony

experimental part, p. 432 - 438 (2009/05/27)

A practical and efficient α-selective aromatic glycosylation with simple per-O-acetyl glycopyranosyl trichloroacetimidates is reported. The method is particularly effective for L-fucosyl and 2-azido-2-deoxy-d-galatosaminyl imidates, with which exclusive α-selectivity was achieved. The synthetic utility of this method was demonstrated in the stereoselective synthesis of 4-methylumbelliferyl α-T-antigen.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 1147438-59-2