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65619-31-0

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65619-31-0 Usage

Description

4-CYANO-4-(2,4-DICHLOROPHENYL)CYCLOHEXANONE is a cyclohexanone derivative featuring a cyano and dichlorophenyl group attached to the cyclohexanone ring. It is a white to light yellow solid that serves as an intermediate in the synthesis of various organic compounds. The chemical structure and functional groups present in the molecule contribute to its utility in the development of pharmaceuticals, agrochemicals, and other fine chemicals. Its reactivity and versatility in forming chemical bonds make it a valuable building block in organic synthesis. Overall, 4-CYANO-4-(2,4-DICHLOROPHENYL)CYCLOHEXANONE is an important compound in the field of organic chemistry with applications across different industries.

Uses

Used in Pharmaceutical Industry:
4-CYANO-4-(2,4-DICHLOROPHENYL)CYCLOHEXANONE is used as a key intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of new drugs with potential therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical sector, 4-CYANO-4-(2,4-DICHLOROPHENYL)CYCLOHEXANONE is utilized as a precursor in the production of agrochemicals, aiding in the creation of compounds that can enhance crop protection and yield.
Used in Fine Chemicals Industry:
4-CYANO-4-(2,4-DICHLOROPHENYL)CYCLOHEXANONE is employed as a building block in the synthesis of fine chemicals, where its unique structure and reactivity are leveraged to produce specialty chemicals for various applications.
Used in Organic Synthesis:
As a versatile intermediate, 4-CYANO-4-(2,4-DICHLOROPHENYL)CYCLOHEXANONE is used in organic synthesis to form a wide range of chemical compounds, showcasing its reactivity and importance in creating new molecules for research and commercial purposes.

Check Digit Verification of cas no

The CAS Registry Mumber 65619-31-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,6,1 and 9 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 65619-31:
(7*6)+(6*5)+(5*6)+(4*1)+(3*9)+(2*3)+(1*1)=140
140 % 10 = 0
So 65619-31-0 is a valid CAS Registry Number.

65619-31-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2,4-dichlorophenyl)-4-oxocyclohexane-1-carbonitrile

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:65619-31-0 SDS

65619-31-0Relevant articles and documents

4-Amino-4-arylcyclohexanones and Their Derivatives, a Novel Class of Analgesics. 1. Modification of the Aryl Ring

Lednicer, Daniel,VonVoigtlander, Philip F.,Emmert, D. Edward

, p. 424 - 430 (2007/10/02)

Investigation of central nervous system activity of phenylcyclohexylamines was continued by preparation of "reversed" analogues.Following the unexpected finding of analgesic activity with 1-(dimethylamino)-1-phenylcyclohexylamine, the SAR of the series was investigated.Synthesis starts by double Michael reaction of acrylate on arylacetonitriles.Following cyclization, decarboxylation, ketalization, and saponification, the geminally substituted acid is rearranged to the isocyanate by means of (C6H5O)2PON3.Isocyanates were then converted to the title compounds.Analgesic activity is very sensitive to the nature and position of the substituent on the aromatic ring.The most potent compounds in this series (p-CH3, p-Br) showed 50percent the potency of morphine.Deletion of the ring oxygen abolishes activity.

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