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2,5-diethyl-4-hydroxy-3,4-diphenylcyclopent-2-en-1-one is a complex organic compound characterized by its unique molecular structure. It features a cyclopent-2-en-1-one ring, which is a five-membered ring with a ketone group at position 1 and a double bond between positions 2 and 3. The molecule also contains two ethyl groups at positions 2 and 5, and two phenyl groups at positions 3 and 4. The presence of a hydroxyl group at position 4 adds to its complexity. 2,5-diethyl-4-hydroxy-3,4-diphenylcyclopent-2-en-1-one is known for its potential applications in the synthesis of various pharmaceuticals and other chemical products due to its diverse functional groups and structural features.

5323-83-1

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5323-83-1 Usage

Chemical Class

Benzyl phenyl ethers

Chemical Structure

Main Structure: Cyclopent-2-en-1-one ring with substitutions
Substitutions:
Two ethyl groups (2,5-diethyl)
Hydroxy group (4-hydroxy)
Two phenyl groups (3,4-diphenyl)

Appearance

Yellow crystalline

Odor

Floral, rose-like

Usage

Fragrance ingredient in cosmetic and personal care products

Safety Precautions

Handle with care
May cause skin irritation
Keep away from heat, sparks, and open flames

Check Digit Verification of cas no

The CAS Registry Mumber 5323-83-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,2 and 3 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5323-83:
(6*5)+(5*3)+(4*2)+(3*3)+(2*8)+(1*3)=81
81 % 10 = 1
So 5323-83-1 is a valid CAS Registry Number.

5323-83-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,5-diethyl-4-hydroxy-3,4-diphenylcyclopent-2-en-1-one

1.2 Other means of identification

Product number -
Other names 2,5-diethyl-4-hydroxy-3,4-diphenyl-cyclopent-2-enone

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:5323-83-1 SDS

5323-83-1Relevant academic research and scientific papers

Pd(II)-Catalyzed Enantioselective Desymmetrization of Polycyclic Cyclohexenediones: Conjugate Addition versus Oxidative Heck

Lamb, Claire J. C.,Vilela, Filipe,Lee, Ai-Lan

supporting information, p. 8689 - 8694 (2019/11/03)

Pd(II)-catalyzed desymmetrization of polycyclic cyclohexenediones has been achieved with high enantio- and diastereoselectivities. Up to five contiguous stereocenters are desymmetrized, while simultaneously, an additional stereocenter is created by the enantioselective conjugate addition. Surprisingly, the conjugate addition products dominate even under typical oxidative Heck conditions, and these observations may provide some insight into the competition between the two related reactions.

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