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57783-86-5

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57783-86-5 Usage

Description

Benzyl 4,6-O-benzylidene-alpha-D-galactopyranoside is a complex organic compound that serves as a valuable intermediate in the field of organic synthesis. It is characterized by its unique chemical structure, which includes a benzyl group and a galactopyranoside moiety connected through a benzylidene bridge.

Uses

Used in Organic Synthesis:
Benzyl 4,6-O-benzylidene-alpha-D-galactopyranoside is used as a synthetic intermediate for the development of various organic compounds. Its unique structure allows for the creation of a wide range of molecules with potential applications in different industries, such as pharmaceuticals, agrochemicals, and materials science.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, Benzyl 4,6-O-benzylidene-alpha-D-galactopyranoside is used as a key building block for the synthesis of complex carbohydrate-based drugs and drug candidates. Its ability to form various derivatives makes it a versatile component in the development of novel therapeutic agents.
Used in Agrochemical Industry:
Benzyl 4,6-O-benzylidene-alpha-D-galactopyranoside is also utilized in the agrochemical industry for the synthesis of bioactive compounds with potential applications in pest control and crop protection. Its unique structure can be modified to create molecules with specific biological activities, contributing to the development of more effective and environmentally friendly agrochemicals.
Used in Materials Science:
In the field of materials science, Benzyl 4,6-O-benzylidene-alpha-D-galactopyranoside can be used as a component in the development of advanced materials with unique properties. Its ability to form various derivatives allows for the creation of materials with tailored characteristics, such as improved mechanical strength, thermal stability, or biocompatibility.

Check Digit Verification of cas no

The CAS Registry Mumber 57783-86-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,7,8 and 3 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 57783-86:
(7*5)+(6*7)+(5*7)+(4*8)+(3*3)+(2*8)+(1*6)=175
175 % 10 = 5
So 57783-86-5 is a valid CAS Registry Number.

57783-86-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name Benzyl 4,6-O-benzylidene-a-D-galactopyranoside

1.2 Other means of identification

Product number -
Other names -

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:57783-86-5 SDS

57783-86-5Relevant articles and documents

Exploring the Biochemical Foundations of a Successful GLUT1-Targeting Strategy to BNCT: Chemical Synthesis and in Vitro Evaluation of the Entire Positional Isomer Library of ortho-Carboranylmethyl-Bearing Glucoconjugates

Matovi?, Jelena,J?rvinen, Juulia,Sokka, Iris K.,Imlimthan, Surachet,Raitanen, Jan-Erik,Montaser, Ahmed,Maaheimo, Hannu,Huttunen, Kristiina M.,Per?niemi, Sirpa,Airaksinen, Anu J.,Sarparanta, Mirkka,Johansson, Mikael P.,Rautio, Jarkko,Ekholm, Filip S.

, p. 285 - 304 (2020/12/21)

Boron neutron capture therapy (BNCT) is a noninvasive binary therapeutic modality applicable to the treatment of cancers. While BNCT offers a tumor-targeting selectivity that is difficult to match by other means, the last obstacles preventing the full har

Synthesis of the trisaccharide repeating unit of capsular polysaccharide from Klebsiella pneumoniae

Susanto, Woen,Kong, Kah-Hoe,Hua, Kuo-Feng,Wu, Shih-Hsiung,Lam, Yulin

, p. 288 - 291 (2019/01/04)

The incidences of primary, pyrogenic liver abscess complicated by meningitis and septic endophthalmitis caused by Klebsiella pneumoniae has increased globally. Earlier studies have shown that the capsular polysaccharide (CPS) of Klebsiella pneumoniae plays an important role in the resistance to phagocytosis and related pathogenicity. The first chemical synthesis of the trisaccharide repeating unit of this CPS has been achieved via stereoselective glycosylation with orthogonal and appropriate protecting groups. A new method for the pyruvylation of trans diol was developed.

TANNIN INHIBITORS OF HIV

-

, (2013/10/07)

The invention provides a method to prevent or treat HIV-infection with synthetic tannins, and pharmaceutical compositions comprising synthetic tannins.

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