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5-phenyl-8H-phthalazino[1,2-b]quinazolin-8-one is a complex organic compound belonging to the phthalazine and quinazoline chemical classes. It is characterized by a unique molecular structure, featuring a phthalazine ring fused to a quinazoline ring, with a phenyl group attached at the 5th position. 5-phenyl-8H-phthalazino[1,2-b]quinazolin-8-one has the molecular formula C20H13N3O and a molecular weight of 309.34 g/mol. It is known for its potential applications in medicinal chemistry, particularly as a scaffold for the development of new drugs targeting various biological pathways. The compound's properties, such as solubility, stability, and reactivity, make it a promising candidate for further research and development in the pharmaceutical industry.

5529-94-2

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5529-94-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5529-94-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,2 and 9 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5529-94:
(6*5)+(5*5)+(4*2)+(3*9)+(2*9)+(1*4)=112
112 % 10 = 2
So 5529-94-2 is a valid CAS Registry Number.
InChI:InChI=1/C22H28N2O3/c1-15-5-6-16(2)21(11-15)23-18-7-9-24(10-8-18)22(25)17-12-19(26-3)14-20(13-17)27-4/h5-6,11-14,18,23H,7-10H2,1-4H3

5529-94-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (3,5-dimethoxyphenyl)-[4-(2,5-dimethylanilino)piperidin-1-yl]methanone

1.2 Other means of identification

Product number -
Other names 5-Phenyl-8-oxo-8H-phthalazino<1,2-b>chinazolin

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:5529-94-2 SDS

5529-94-2Downstream Products

5529-94-2Relevant academic research and scientific papers

Anthranilic acid hydrazide in the synthesis of fused polycyclic compounds with quinazoline moieties

Ukhin,Kuz'Mina,Gribanov,Belousova,Orlova

, p. 2340 - 2348 (2008)

A modified procedure was developed for the synthesis of 5,6,7,8,13,13a-hexahydrophthalazino[1,2-b]quinazoline-5,8-dione and 6-amino-5,6,6a,11-tetrahydroisoindolo[2,1-a]quinazoline-5,11-dione from o-formylbenzoic acid and anthranilic acid hydrazide. The mechanism of the transformation is suggested, some reactions were studied, and new derivatives of these compounds were synthesized. Anthranilic acid hydrazide was used in the novel synthesis of 5-substituted phthalazino[1,2-b]quinazolin-8-one derivatives. The possible reaction mechanism is discussed. 5,6,7,8-Tetrahydrophthalazino[1, 2-b]quinazoline-5,8-dione and 5-phenylphthalazino[2,1-b]quinazolin-8-one were studied by X-ray diffraction.

Synthesis and biological activity of 5-substituted 8-oxo-8H-phthalazinoquinazolines

Razvi, Mehboob,Ramalingam, T,Sattur, P B

, p. 399 - 400 (2007/10/02)

Several 5-substituted 8-oxo-8H-phthalazinoquinazolines (3) have been synthesised by the reaction of 4-substituted 1-chlorophthalazines (1) with anthranilic acid (2).These compounds have been screened for their antiinflammatory, antihypertensive and motor activities.Few compounds exhibit markled antiinflammatory activity.

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