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(4-(beta-D-Glucopyranosyloxy)phenyl)phenylmethanone hemihydrate is a chemical compound characterized by a phenyl ring with a glucopyranose group attached and a phenylmethanone moiety. It exists in a hemihydrate form, which means it contains one molecule of water for every two molecules of the compound. (4-(beta-D-Glucopyranosyloxy)phenyl)phenylmethanone hemihydrate is known for its potential biological activity and ability to interact with enzymes and receptors, making it a promising candidate for pharmaceutical and research applications.

83355-65-1

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83355-65-1 Usage

Uses

Used in Pharmaceutical Applications:
(4-(beta-D-Glucopyranosyloxy)phenyl)phenylmethanone hemihydrate is used as a pharmaceutical compound for its potential biological activity and ability to interact with enzymes and receptors. Its unique structure allows it to be a promising candidate for drug development and therapeutic interventions.
Used in Research Applications:
In the field of research, (4-(beta-D-Glucopyranosyloxy)phenyl)phenylmethanone hemihydrate is used as a chemical compound for studying its interactions with enzymes and receptors. This helps in understanding its potential applications in drug development and therapeutic interventions, contributing to the advancement of medical science.
Used in Drug Development:
(4-(beta-D-Glucopyranosyloxy)phenyl)phenylmethanone hemihydrate is used as a key component in drug development due to its potential biological activity and ability to interact with enzymes and receptors. Its unique structure and properties make it a valuable asset in the creation of new therapeutic interventions.
Used in Therapeutic Interventions:
As a compound with potential biological activity, (4-(beta-D-Glucopyranosyloxy)phenyl)phenylmethanone hemihydrate is used in therapeutic interventions to target specific enzymes and receptors. This can lead to the development of novel treatments for various medical conditions, improving patient outcomes and overall healthcare.

Check Digit Verification of cas no

The CAS Registry Mumber 83355-65-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,3,5 and 5 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 83355-65:
(7*8)+(6*3)+(5*3)+(4*5)+(3*5)+(2*6)+(1*5)=141
141 % 10 = 1
So 83355-65-1 is a valid CAS Registry Number.
InChI:InChI=1/C19H20O7/c20-10-14-16(22)17(23)18(24)19(26-14)25-13-8-6-12(7-9-13)15(21)11-4-2-1-3-5-11/h1-9,14,16-20,22-24H,10H2/t14-,16-,17+,18-,19-/m1/s1

83355-65-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name phenyl-[4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]methanone

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:83355-65-1 SDS

83355-65-1Downstream Products

83355-65-1Relevant academic research and scientific papers

Glycosylated Derivatives of Benzophenone, Benzhydrol, and Benzhydril as Potential Venous Antithrombotic Agents

Bellamy, Francois,Horton, Derek,Millet, Jean,Picart, Francois,Samreth, Soth,Chazan, Jean Bernard

, p. 898 - 903 (2007/10/02)

A series of glycosylated derivatives of benzophenone, benzhydrol, and benzhydril has been synthesized and evaluated for potential activity as venous antithrombotic agents.Studies on structure-activity relationships revealed that compounds having an electr

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