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1(2H)-Phthalazinone, 4-(4-chloro-3-methylphenyl)-5,6,7,8-tetraphenylis a complex chemical compound belonging to the phthalazinone derivatives. It is distinguished by its phthalazinone core structure, to which four phenyl rings are attached at various positions. 1(2H)-Phthalazinone, 4-(4-chloro-3-methylphenyl)-5,6,7,8-tetraphenylalso features a 4-chloro-3-methylphenyl group, contributing to its unique structural characteristics. 1(2H)-Phthalazinone, 4-(4-chloro-3-methylphenyl)-5,6,7,8-tetraphenylholds promise in the realms of organic synthesis and medicinal chemistry, owing to its potential biological activities and distinctive molecular architecture. Further investigation is required to fully understand its properties and explore its possible applications.

129352-68-7

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129352-68-7 Usage

Uses

Used in Organic Synthesis:
1(2H)-Phthalazinone, 4-(4-chloro-3-methylphenyl)-5,6,7,8-tetraphenylis used as a key intermediate in the synthesis of various organic compounds. Its unique structural features make it a valuable building block for creating novel molecules with specific properties and functions.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 1(2H)-Phthalazinone, 4-(4-chloro-3-methylphenyl)-5,6,7,8-tetraphenylis utilized as a potential candidate for the development of new drugs. Its structural diversity and potential biological activities suggest that it may be instrumental in the design and synthesis of pharmaceuticals targeting specific medical conditions.
Used in Research and Development:
1(2H)-Phthalazinone, 4-(4-chloro-3-methylphenyl)-5,6,7,8-tetraphenylis also employed in research and development settings, where it can be used to study the effects of structural modifications on the properties and activities of phthalazinone derivatives. This knowledge can be applied to optimize the compound for specific applications, such as improving its stability, solubility, or bioavailability.
Used in Chemical Analysis:
1(2H)-Phthalazinone, 4-(4-chloro-3-methylphenyl)-5,6,7,8-tetraphenylcan be utilized in chemical analysis to understand the interactions between different molecular components. This information can be crucial for the development of new analytical methods or the improvement of existing ones.
Used in Material Science:
In material science, 1(2H)-Phthalazinone, 4-(4-chloro-3-methylphenyl)-5,6,7,8-tetraphenylmay be investigated for its potential to enhance the properties of various materials, such as improving their mechanical strength, thermal stability, or chemical resistance.

Check Digit Verification of cas no

The CAS Registry Mumber 129352-68-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,3,5 and 2 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 129352-68:
(8*1)+(7*2)+(6*9)+(5*3)+(4*5)+(3*2)+(2*6)+(1*8)=137
137 % 10 = 7
So 129352-68-7 is a valid CAS Registry Number.

129352-68-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(4-chloro-3-methylphenyl)-5,6,7,8-tetraphenyl-2H-phthalazin-1-one

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

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More Details:129352-68-7 SDS

129352-68-7Relevant academic research and scientific papers

SYNTHESIS OF 4,5,6,7-TETRAPHENYL-8(SUBSTITUTED-3(2H)-PHTHALAZINONE DERIVATIVES WITH POTENTIAL ANTIHYPERTENSIVE ACTIVITY

Yassin, F. A.,El-Safty, M. A.,Bayoumy, B. E.,Farargy, A. F. El

, p. 201 - 208 (2007/10/03)

The interaction of tetraphenylphthalic anhydride with o-chlorotoluene under Friedel-Crafts conditions gives 2-(4-chloro-3-methyl)benzoyl-3,4,5,6-tetraphenyl benzoic acid (1) which on reaction with hydrazine derivatives gave phthalazinones 2a-d. The behaviour of 2a towards carbon electrophiles and carbon nucleophiles has been investigated. The chlorophthalazinone 3s has been also synthesised through the action of PCl5/POCl3 on 2a. The behaviour of 3s towards nitrogen, and oxygen nucleophiles also has been described.

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