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[(4Z)-4-(hydroxyimino)-3-methylcyclohexa-2,5-dien-1-ylidene](phenyl)acetonitrile, a chemical compound with the molecular formula C15H13N3O, is a yellow solid that belongs to the nitrile family. It features a phenyl group and a hydroxyimino functional group, making it a valuable building block in the synthesis of various organic compounds. This versatile compound holds significance in organic chemistry, with potential applications in medicinal chemistry and material science.

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Uses

Used in Organic Synthesis:
[(4Z)-4-(hydroxyimino)-3-methylcyclohexa-2,5-dien-1-ylidene](phenyl)acetonitrile is used as a building block for the synthesis of various organic compounds due to its unique structure and functional groups. Its ability to form meta-depside bonds and interact with biopolymers and macromolecules makes it a promising candidate for creating novel molecules with specific properties and applications.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, [(4Z)-4-(hydroxyimino)-3-methylcyclohexa-2,5-dien-1-ylidene](phenyl)acetonitrile is used as a key intermediate for the development of new pharmaceuticals. Its structural features allow for the design and synthesis of potential drug candidates that can modulate various biological pathways and target specific diseases.
Used in Material Science:
[(4Z)-4-(hydroxyimino)-3-methylcyclohexa-2,5-dien-1-ylidene](phenyl)acetonitrile also finds application in material science, where it can be utilized to create novel materials with specific properties. Its phenyl group and hydroxyimino functional group can contribute to the development of materials with enhanced stability, reactivity, or other desired characteristics.
Overall, [(4Z)-4-(hydroxyimino)-3-methylcyclohexa-2,5-dien-1-ylidene](phenyl)acetonitrile is a versatile and important compound in the field of organic chemistry, with potential applications in various industries, including organic synthesis, medicinal chemistry, and material science. Its precise properties and uses depend on the specific research or industrial context in which it is employed.

Check Digit Verification of cas no

The CAS Registry Mumber 728-65-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,2 and 8 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 728-65:
(5*7)+(4*2)+(3*8)+(2*6)+(1*5)=84
84 % 10 = 4
So 728-65-4 is a valid CAS Registry Number.

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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 (2Z)-2-[(4Z)-4-hydroxyimino-3-methylcyclohexa-2,5-dien-1-ylidene]-2-phenylacetonitrile

1.2 Other means of identification

Product number -
Other names <4-Hydroxyimino-3-methyl-cyclohexyl-2,5-dienyliden>-phenyl-acetonitril

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:728-65-4 SDS

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728-65-4Relevant academic research and scientific papers

Solvent-free mechanochemical synthesis of arylcyanomethylenequinone oximes from phenylacetonitriles and 4-unsubstituted nitroaromatic compounds using KF/nano-γ-Al2O3 as catalyst

Hong, Zhi,Li, Jian-Jun,Chen, Guang,Jiang, Hua-Jiang,Yang, Xiao-Feng,Pan, Heng,Su, Wei-Ke

, p. 13581 - 13588 (2016/02/12)

Solvent-free condensation of phenylacetonitriles with 4-unsubstituted nitroaromatic compounds to produce a series of arylcyanomethylenequinone oximes was described in the presence of KF/nano-γ-Al2O3 under high-speed vibration milling

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