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2,3,4,6-tetra-O-acetyl-1-O-[(1E)-2,2,2-trichloroethanimidoyl]hexopyranose is a complex acetylated hexopyranose derivative with a trichloroethanimidoyl group attached to the sugar molecule. 2,3,4,6-tetra-O-acetyl-1-O-[(1E)-2,2,2-trichloroethanimidoyl]hexopyranose features multiple functional groups, including acetyl and imine groups, as well as three chlorine atoms, making it a versatile molecule for various applications in organic chemistry, biochemistry, and pharmaceutical research.

6047-47-8

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6047-47-8 Usage

Uses

Used in Organic Chemistry:
2,3,4,6-tetra-O-acetyl-1-O-[(1E)-2,2,2-trichloroethanimidoyl]hexopyranose is used as a synthetic intermediate for the preparation of various complex organic compounds. Its multiple functional groups allow for further chemical modifications and reactions, making it a valuable building block in organic synthesis.
Used in Biochemistry:
In biochemistry, 2,3,4,6-tetra-O-acetyl-1-O-[(1E)-2,2,2-trichloroethanimidoyl]hexopyranose can be used as a probe or inhibitor for studying enzyme activity and interactions with biomolecules. Its unique structure and functional groups enable selective binding and modulation of specific biological targets.
Used in Pharmaceutical Research:
2,3,4,6-tetra-O-acetyl-1-O-[(1E)-2,2,2-trichloroethanimidoyl]hexopyranose is used as a potential drug candidate or lead compound in pharmaceutical research. Its complex structure and multiple functional groups can be optimized for specific therapeutic targets, such as enzymes or receptors, to develop new drugs with improved efficacy and selectivity.
Used in Chemical Synthesis Industry:
2,3,4,6-tetra-O-acetyl-1-O-[(1E)-2,2,2-trichloroethanimidoyl]hexopyranose is used as a key intermediate in the synthesis of various specialty chemicals, including pharmaceuticals, agrochemicals, and materials. Its unique structure and functional groups make it a valuable component in the development of novel and innovative products.
Used in Research and Development:
In the research and development sector, 2,3,4,6-tetra-O-acetyl-1-O-[(1E)-2,2,2-trichloroethanimidoyl]hexopyranose serves as a valuable tool for exploring new chemical reactions, mechanisms, and applications. Its complex structure and multiple functional groups provide opportunities for advancing scientific knowledge and discovering new uses for this versatile compound.

Check Digit Verification of cas no

The CAS Registry Mumber 6047-47-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,4 and 7 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6047-47:
(6*6)+(5*0)+(4*4)+(3*7)+(2*4)+(1*7)=88
88 % 10 = 8
So 6047-47-8 is a valid CAS Registry Number.

6047-47-8SDS

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 1,3-bis(4-tolylthio)propan-2-ol

1.2 Other means of identification

Product number -
Other names 1,3-bis(p-tolylthio)propan-2-ol

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:6047-47-8 SDS

6047-47-8Downstream Products

6047-47-8Relevant academic research and scientific papers

Selective synthesis of 4-thiomethyl-1,3-dioxolan-2-ones under microwave irradiation using an environmentally benign KF/Al2O3/PEG-400 system

Perin, Gelson,Silva, Cristian M.,Borges, Elton L.,Duarte, José E. G.,Goulart, Helen A.,Silva, Rafaela B.,Schumacher, Ricardo F.

, p. 5873 - 5885 (2016/06/01)

We describe a simple and rapid method for selective synthesis of 4-thiomethyl-1,3-dioxolan-2-ones promoted by KF/Al2O3 using PEG-400 as solvent under microwave irradiation. The protocol employs 3-O-tosyl glycerol 1,2-carbonate 1 and

Radical-induced 1,3-Rearrangemets of Allylic Sulfones bearing an Alkylthio or Arylthio Substituent at the α-Position

Fox, Judith M.,Morris, Clare M.,Smyth, G. Darren,Whitman, Gordon H.

, p. 731 - 738 (2007/10/02)

1-Methylthio-1-p-tolylsulfonylprop-2-ene 2 underwent 1,3-rearrangement under conditions of radical initiation with migration of the p-tolylsulfonyl group by a process considered to have involved addition-elimination of arylsulfonyl radicals.In contrast, t

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