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2-acetyl-1,5-anhydro-2,4-dideoxy-3-C-methyl-1,5-diphenyl-1-thiopentitol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

92760-85-5

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92760-85-5 Usage

Functional Groups

Acetyl group: Provides chemical reactivity and can participate in acylation reactions.
Anhydro group: Confers cyclic structure and potential reactivity in dehydration reactions.
Dideoxy group: Indicates the absence of two hydroxyl groups in the sugar moiety, altering its properties.
Methyl group: Introduces steric effects and influences the compound's conformational preferences.
Diphenyl group: Imparts aromaticity and influences the compound's solubility and interactions.
Thiopentitol group: Contains a sulfur atom, which can contribute to unique chemical properties such as thiol reactivity.

Potential Chemical Properties

Reactivity in acylation and dehydration reactions.
Altered sugar moiety properties due to the absence of two hydroxyl groups.
Steric effects and conformational preferences influenced by the methyl group.
Aromaticity and potential π-π interactions mediated by the diphenyl group.
Unique chemical reactivity associated with the sulfur atom in the thiopentitol group.

Potential Applications

Drug development: Due to its diverse chemical properties, it could be explored for medicinal purposes.
Chemical synthesis: May serve as a building block for the synthesis of other complex molecules.
Material science: Could be investigated for applications in materials with tailored properties.

Research Needs

Further studies are required to elucidate its specific chemical reactivity and potential applications.
Understanding its behavior in different reaction conditions and environments is necessary.
Exploring its interactions with biological systems and assessing any pharmacological potential is warranted.

Check Digit Verification of cas no

The CAS Registry Mumber 92760-85-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,7,6 and 0 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 92760-85:
(7*9)+(6*2)+(5*7)+(4*6)+(3*0)+(2*8)+(1*5)=155
155 % 10 = 5
So 92760-85-5 is a valid CAS Registry Number.

92760-85-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-hydroxy-4-methyl-2,6-diphenylthian-3-yl)ethanone

1.2 Other means of identification

Product number -
Other names 4-hydroxy-4-methyl-2,6-diphenyl-5-acetyl-thiane

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:92760-85-5 SDS

92760-85-5Downstream Products

92760-85-5Relevant academic research and scientific papers

Phase Transfer-Catalyzed Reactions between Polysulfide Anions and α,β-Unsaturated Carbonyl Compounds

Krein, Eitan B.,Aizenshtat, Zeev

, p. 6103 - 6108 (2007/10/02)

Ammonium polysulfide reacts with α,β-unsaturated ketones and aldehydes under PTC (phase transfer catalysis) conditions in a rather different manner than it does in homogeneous systems. 1,3-Diphenyl-2-propen-1-one (chalcone, 1) and 4-phenyl-3-buten-2-one (

Variable Reaction Pathways for the Action of Polysulfide on Michael Acceptors

LaLonde, Robert T.,Florence, Robert A.,Horenstein, Benjamin A.,Fritz, Richard C.,Silveira, Linda,et al.

, p. 85 - 91 (2007/10/02)

α,β-Unsaturated enones and cinnamaldehyde are treated with ethanolic sodium polysulfide and the product mixtures are analyzed to ascertain the types of products. 2'-Methoxychalcone reacts to give a thiolane wherein C-2 of one chalcone unit forms a carbon-

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