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1(2H)-Phthalazinone, 2-(2-hydroxyethyl)-4-phenylis a chemical compound with the molecular formula C15H13NO2. It is derived from the phthalazinone molecule and features a hydroxyethyl group and a phenyl group. 1(2H)-Phthalazinone, 2-(2-hydroxyethyl)-4-phenylhas been studied for its potential biological and pharmacological activities, including its use as a potential anti-inflammatory and anti-cancer agent. It is also utilized as an intermediate in the production of various organic compounds, making it a versatile and significant chemical in the fields of medicine and industry.

3306-76-1

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3306-76-1 Usage

Uses

Used in Pharmaceutical Synthesis:
1(2H)-Phthalazinone, 2-(2-hydroxyethyl)-4-phenylis used as a key intermediate in the synthesis of pharmaceuticals for its potential anti-inflammatory and anti-cancer properties. Its unique structure allows for the development of new drugs that can target specific biological pathways.
Used in Polymer and Resin Production:
In the chemical industry, 1(2H)-Phthalazinone, 2-(2-hydroxyethyl)-4-phenylis used as an intermediate in the production of polymers and resins. Its chemical properties contribute to the development of materials with specific characteristics, such as enhanced strength, durability, or flexibility.
Used in Organic Compound Production:
1(2H)-Phthalazinone, 2-(2-hydroxyethyl)-4-phenylis also utilized as an intermediate in the production of various organic compounds, highlighting its versatility in different chemical reactions and applications across the industry.

Check Digit Verification of cas no

The CAS Registry Mumber 3306-76-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,0 and 6 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3306-76:
(6*3)+(5*3)+(4*0)+(3*6)+(2*7)+(1*6)=71
71 % 10 = 1
So 3306-76-1 is a valid CAS Registry Number.

3306-76-1Relevant academic research and scientific papers

1-Hydroxyethylpyridazin-6-ones and their O-acetyl- and O-diphenylphosphinoyl derivatives

Bagrov,Petrukhina

, p. 1520 - 1522 (2007/10/03)

Condensation of 2-hydroxyethylhydrazine with 2-acetyl-, 2-phenylacetyl-, and 2-benzoylbenzoic and α-oxoglutaric acids yields 1-hydroxyethylpyridazin-6-one derivatives. The hydroxy group in 2-hydroxyethylphthalazin-1-ones can readily be acetylated and phos

The effect of conformational equilibrium on rate of reactions involving neighbouring group participation

Csampai,Farkas

, p. 1507 - 1514 (2007/10/02)

The hydrolysis reaction of condensed bromoalkylphthalazinones type 4 is efficiently assisted by the neighbouring hydrazinocarbonyl group. The expected order of anchimeric assistance has been found to be dependent on the chain length. The relatively large

BROMOALKYLPHTALAZINONES AND ISOMERIC OXAZOLINIUM SALTS AS INTERMEDIATES AND SYNTHONS

Csampai, A.,Koermendy, K.,Sohar, P.,Ruff. F.

, p. 5539 - 5548 (2007/10/02)

2(ο-Piperidinoalkyl)phtalazin-1(2H)-ones can be prepared from the 2-hydroxyalkyl compounds both via the open-chain 2-bromoalkyl derivatives and via their cyclic isomers.Substitution reactions of bromoalkyl compounds may be assisted by polar solvents and b

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