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8-phenyl-7H-purine is an organic compound with the molecular formula C12H9N5. It is a derivative of purine, a heterocyclic aromatic organic compound consisting of a pyrimidine ring fused to an imidazole ring. The 8-phenyl substitution refers to a phenyl group (C6H5) attached to the 8th position of the purine ring. 8-phenyl-7H-purine is of interest in medicinal chemistry and may have potential applications in the development of drugs targeting purine-related metabolic pathways, such as those involved in the treatment of gout or certain types of cancer. Its chemical structure and properties make it a subject of study for researchers exploring the interactions of purine analogs with enzymes and receptors in the body.

4776-14-1

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4776-14-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4776-14-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,7,7 and 6 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 4776-14:
(6*4)+(5*7)+(4*7)+(3*6)+(2*1)+(1*4)=111
111 % 10 = 1
So 4776-14-1 is a valid CAS Registry Number.

4776-14-1SDS

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 8-phenyl-7H-purine

1.2 Other means of identification

Product number -
Other names 8-phenylpurine

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:4776-14-1 SDS

4776-14-1Downstream Products

4776-14-1Relevant academic research and scientific papers

Nickel catalyzed sustainable synthesis of benzazoles and purines: Via acceptorless dehydrogenative coupling and borrowing hydrogen approach

Chakraborty, Gargi,Guin, Amit Kumar,Mondal, Rakesh,Paul, Nanda

, p. 7217 - 7233 (2021/08/30)

Herein we report nickel-catalyzed sustainable synthesis of a few chosen five-membered fused nitrogen heterocycles such as benzimidazole, purine, benzothiazole, and benzoxazole via acceptorless dehydrogenative functionalization of alcohols. Using a bench stable, easy to prepare, and inexpensive Ni(ii)-catalyst, [Ni(MeTAA)] (1a), featuring a tetraaza macrocyclic ligand (tetramethyltetraaza[14]annulene (MeTAA)), a wide variety of polysubstituted benzimidazole, purine, benzothiazole, and benzoxazole derivatives were prepared via dehydrogenative coupling of alcohols with 1,2-diaminobenzene, 4,5-diaminopyrimidine, 2-aminothiphenol, and 2-aminophenol, respectively. A wide array of benzimidazoles were also prepared via a borrowing hydrogen approach involving alcohols as hydrogen donors and 2-nitroanilines as hydrogen acceptors. A few control experiments were performed to understand the reaction mechanism.

Oxidative Cyclization Approach to Benzimidazole Libraries

Arnold, Eric P.,Mondal, Prolay K.,Schmitt, Daniel C.

supporting information, p. 1 - 5 (2020/02/20)

An efficient approach to the parallel synthesis of benzimidazoles from anilines is described. Library approaches to vary the N1 and C2 vectors of benzimidazoles are well established; however, C4-C7 variation has traditionally relied on 1,2-dianiline build

An electroluminescent compound and an electroluminescent device comprising the same

-

Paragraph 0474; 0475; 0537; 0538, (2016/10/07)

The present invention relates to an organic light emitting compound applied to an organic light emitting device. The organic light emitting compound: is represented by chemical formula 1; includes one or more substituted bodies represented by structural formula 1 or structural formula 2; and is capable of realizing an organic light emitting device having excellent luminous properties such as driving voltage, luminance, a long life and the like in the case of being applied as a phosphorescent host compound in a hole transporting functional layer or an emissive layer.COPYRIGHT KIPO 2016

Microwave-assisted one step high-throughput synthesis of benzimidazoles

Lin, Shou-Yuan,Isome, Yuko,Stewart, Ethan,Liu, Ji-Feng,Yohannes, Daniel,Yu, Libing

, p. 2883 - 2886 (2007/10/03)

One-pot synthesis of benzimidazoles from diamines and carboxylic acids was developed under microwave irradiation condition, which provided a practical and efficient method for high-throughput synthesis of this important class of heterocyclic compounds.

Selective C-arylation of free (NH)-heteroarenes via catalytic C-H bond functionalization

Sezen, Bengue,Sames, Dalibor

, p. 5274 - 5275 (2007/10/03)

A new system for palladium-catalyzed arylation of a broad spectrum of free (NH)-heteroarenes has been developed (indole, pyrrole, pyrazole, 2-phenylimidazole, imidazole, benzimidazole, and purine). Remarkable selectivity has been achieved in the presence of MgO base, providing single C-arylation products, while no N-arylation and no bis-arylation products have been detected. In the case of free imidazole, exclusive C-4 arylation may be switched to exclusive 2-arylation by the addition of CuI to the Pd/Ph3P/MgO system. When free aryl-(NH)-azoles are desired, direct arylation eliminates three steps in comparison to standard methods, including N-protection, stoichiometric metalation or halogenation, and N-deprotection. Copyright

DEAMINATION, INVOLVING RING OPENING, IN REACTIONS OF 1-AMINOPURINIUM MESITYLENESULFONATES WITH METHANOLIC AMMONIA

Kos, N. J.,Jongejan, H.,van der Plas, H. C.

, p. 4841 - 4848 (2007/10/02)

On reaction of 1-aminopurinium mesitylenesulfonates with methanolic ammonia N-deamination occurs.For 1-amino-, 1-amino-8-(methylthio)-, 1-amino-8-phenyl-, 1-amino-2-methyl-, 1-amino-6-methyl- and 1-amino-8-phenyl-9-methylpurinium mesitylenesulfonate this reaction proceeds for at least 75percent via ring opening as shown by the isolation of 1-15N-labelled purines when 15N-labelled methanolic ammonia was used. 1-Amino-9-methylpurinium mesitylenesulfonate gave N-deamination without ring opening.The reaction of 1-amino-6-(methylthio)purinium mesitylenesulfonate with methanolic ammonia involves, besides deamination, partial substitution of the methylthio group; no ring opening is involved.However, ring opening followed by substitution occurs in the reaction of 1-amino-2-(methylthio)purinium mesitylenesulfonate; the reaction proceeds via an adduct at position 2.

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