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4-Methylphenyl 4,6-O-benzylidene-1-thio-b-D-glucopyranoside is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 868241-49-0 Structure
  • Basic information

    1. Product Name: 4-Methylphenyl 4,6-O-benzylidene-1-thio-b-D-glucopyranoside
    2. Synonyms: 4-Methylphenyl 4,6-O-benzylidene-1-thio-b-D-glucopyranoside;4-METHYLPHENYL 4,6-O-BENZYLIDENE-1-THIO-β-D-GLUCOPYRANOSIDE;4-Methylphenyl 4,6-O-benzylidene-b-D-thioglucopyranoside
    3. CAS NO:868241-49-0
    4. Molecular Formula: C20H22O5S
    5. Molecular Weight: 374.45068
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 868241-49-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 4-Methylphenyl 4,6-O-benzylidene-1-thio-b-D-glucopyranoside(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-Methylphenyl 4,6-O-benzylidene-1-thio-b-D-glucopyranoside(868241-49-0)
    11. EPA Substance Registry System: 4-Methylphenyl 4,6-O-benzylidene-1-thio-b-D-glucopyranoside(868241-49-0)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 868241-49-0(Hazardous Substances Data)

868241-49-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 868241-49-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,8,2,4 and 1 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 868241-49:
(8*8)+(7*6)+(6*8)+(5*2)+(4*4)+(3*1)+(2*4)+(1*9)=200
200 % 10 = 0
So 868241-49-0 is a valid CAS Registry Number.

868241-49-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Methylphenyl 4,6-O-benzylidene-1-thio-b-D-glucopyranoside

1.2 Other means of identification

Product number -
Other names 4-methylphenyl thiophene-2-carboxylate

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:868241-49-0 SDS

868241-49-0Relevant articles and documents

Site-Selective Acylation of Pyranosides with Oligopeptide Catalysts

Seitz, Alexander,Wende, Raffael C.,Roesner, Emily,Niedek, Dominik,Topp, Christopher,Colgan, Avene C.,McGarrigle, Eoghan M.,Schreiner, Peter R.

, p. 3907 - 3922 (2021/03/09)

Herein, we report the oligopeptide-catalyzed site-selective acylation of partially protected monosaccharides. We identified catalysts that invert site-selectivity compared to N-methylimidazole, which was used to determine the intrinsic reactivity, for 4,6

PREPARATION OF MONOSACCHARIDES, DISACCHARIDES, TRISACCHARIDES, AND PENTASACCHARIDES OF HEPARINOIDS

-

, (2017/02/02)

The present invention provides preparations of monosaccharides, disaccharides, trisaccharides, and pentasaccharides of heparinoids. The present invention also provides novel monosaccharides, disaccharides, trisaccharides and pentasaccharides for use in th

Urea–hydrogen peroxide prompted the selective and controlled oxidation of thioglycosides into sulfoxides and sulfones

Singh, Adesh Kumar,Tiwari, Varsha,Mishra, Kunj Bihari,Gupta, Surabhi,Kandasamy, Jeyakumar

, p. 1139 - 1144 (2017/06/20)

A practical method for the selective and controlled oxidation of thioglycosides to corresponding glycosyl sulfoxides and sulfones is reported using urea–hydrogen peroxide (UHP). A wide range of glycosyl sulfoxides are selectively achieved using 1.5 equiv of UHP at 60 °C while corresponding sulfones are achieved using 2.5 equiv of UHP at 80 °C in acetic acid. Remarkably, oxidation susceptible olefin functional groups were found to be stable during the oxidation of sulfide.

Exploring glycosylation reactions under continuous-flow conditions

Cancogni, Damiano,Lay, Luigi

, p. 2873 - 2878 (2015/01/16)

The industrial development of carbohydrate-based drugs is greatly thwarted by the typical challenges inherent in oligosaccharide synthesis. The practical advantages of continuous-flow synthesis in microreactors (high reproducibility, easy scalability, and fast reaction optimization) may offer an effective support to make carbohydrates more attractive targets for drug-discovery processes. Here we report a systematic exploration of the glycosylation reaction carried out under microfluidic conditions. Trichloroacetimidates and thioglycosides have been investigated as glycosyl donors, using both primary and secondary acceptors. Each microfluidic glycosylation has been compared with the corresponding batch reaction, in order to highlight advantages and drawbacks of microreactors technology. As a significant example of multistep continuous-flow synthesis, we also describe the preparation of a trisaccharide by means of two consecutive glycosylations performed in interconnected microreactors.

Highly diastereoselective thioglycosylation of functionalized peracetylated glycosides catalyzed by MoO2Cl2

Weng, Shiue-Shien,Lin, Yow-Dzer,Chen, Chien-Tien

, p. 5633 - 5636 (2007/10/03)

Among 18 oxometallic species, MoO2Cl2 was found to be the most reactive in catalytic thioglycosylation of O-acetylated glycosides with functionalized thiols in CH2Cl2, leading cleanly to 1,2-trans-thioglycosides with exclusive diastereocontrol. The new catalytic protocol is applicable to a monoglycoside building block and β-(1→6)-S-linked-thiodisaccharide synthesis.

Synthesis of 48 disaccharide building blocks for the assembly of a heparin and heparan sulfate oligosaccharide library

Lu, Ng-Dai,Shie, Chi-Rung,Kulkarni, Suvarn S.,Pan, Guan-Rong,Lu, Xin-An,Hung, Shang-Cheng

, p. 5995 - 5998 (2007/10/03)

(Chemical Equation Presented) An efficient synthesis of the entire set of suitably protected 48 disaccharide building blocks for the assembly of a heparin and heparan sulfate oligosaccharide library is described here.

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