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5,6-DIPHENYLFURO[2,3-D]PYRIMIDIN-4-AMINE is a chemical compound characterized by a furo[2,3-d]pyrimidine core structure, which features a pyrimidine ring fused to a furan ring. This derivative of furo[2,3-d]pyrimidine is notable for its two phenyl groups and an amine group attached to the pyrimidine ring. Its unique structure endows it with potential pharmacological activities, positioning it as a promising candidate in medicinal chemistry research for the development of novel drugs. Additionally, it holds significance in the fields of organic synthesis and material science, making it a valuable asset in a range of chemical and pharmaceutical research domains.

5207-52-3

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5207-52-3 Usage

Uses

Used in Medicinal Chemistry Research:
5,6-DIPHENYLFURO[2,3-D]PYRIMIDIN-4-AMINE is used as a chemical intermediate for the synthesis of new drugs due to its potential pharmacological properties. Its unique molecular structure allows for the exploration of various therapeutic applications, including the development of compounds that could target specific biological pathways or receptors.
Used in Organic Synthesis:
In the field of organic synthesis, 5,6-DIPHENYLFURO[2,3-D]PYRIMIDIN-4-AMINE serves as a key building block for the creation of more complex organic molecules. Its presence in synthetic routes can lead to the production of a variety of organic compounds with diverse applications.
Used in Material Science:
5,6-DIPHENYLFURO[2,3-D]PYRIMIDIN-4-AMINE is utilized in material science for the development of new materials with specific properties. Its incorporation into material formulations can contribute to the creation of substances with tailored characteristics for use in various industries, such as electronics, pharmaceuticals, or as specialty chemicals.
Used in Pharmaceutical Development:
5,6-DIPHENYLFURO[2,3-D]PYRIMIDIN-4-AMINE is used as a lead compound in drug discovery for its potential to be optimized into a pharmaceutical agent. Its unique structure may offer new avenues for treating diseases by interacting with biological targets in novel ways.
Used in Chemical Research:
In the broader scope of chemical research, 5,6-DIPHENYLFURO[2,3-D]PYRIMIDIN-4-AMINE is employed as a subject of study to understand its reactivity, stability, and potential interactions with other molecules. This research can provide insights into new chemical reactions or mechanisms that could be applied in various chemical processes.

Check Digit Verification of cas no

The CAS Registry Mumber 5207-52-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,2,0 and 7 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5207-52:
(6*5)+(5*2)+(4*0)+(3*7)+(2*5)+(1*2)=73
73 % 10 = 3
So 5207-52-3 is a valid CAS Registry Number.
InChI:InChI=1/C18H13N3O/c19-17-15-14(12-7-3-1-4-8-12)16(13-9-5-2-6-10-13)22-18(15)21-11-20-17/h1-11H,(H2,19,20,21)

5207-52-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 5,6-Diphenylfuro[2,3-d]pyrimidin-4-amine

1.2 Other means of identification

Product number -
Other names 5,6-diphenylfurano[2,3-d]pyrimidine-4-ylamine

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:5207-52-3 SDS

5207-52-3Downstream Products

5207-52-3Relevant academic research and scientific papers

Fused pyrimidines. Part II: Synthesis and antimicrobial activity of some furo[3,2-e]imidazo[1,2-c]pyrimidines and furo[2,3-d]pyrimidines

Bhuiyan,Rahman, Khandker M. M.,Hossain,Rahim,Hossain

, p. 633 - 636 (2007/10/03)

2-Amino-4,5-diphenylfuran-3-carbonitrile (2) reacted with N-[bis(methylthio)methylene]glycine ethyl ester (1) to afford a double cyclized product 5-methylthio-8,9-diphenylfuro[3,2-e]imidazo[1,2-c]pyrimidin-2(3H)-one (3). Compound 2 also reacts with benzon

COMPOUND FOR INHIBITING TYROSINE KINASE ACTIVITY OF DDR2 PROTEIN

-

Page/Page column 37-38, (2010/02/14)

A new furopyrimidine compound, their pharmaceutically acceptable salt, and a tyrosine kinase activity inhibitor. The furopyrimidine compound is a compound defined by chemical formula 1, 2, 3 or 4, on their precursor, and can exist as a form of free base or in an acid-addition salt. Since the furopyrimidine compound has an effect of inhibiting activity of DDR2 tyrosine kinase, it can be used in treating illnesses caused by the DDR2 tyrosine kinase activity such as hepatocirrhosis, rheumatoid arthritis or cancer.

SYNTHESIS OF HETEROCYCLIC COMPOUNDS FROM THE PRODUCTS OF ADDITION OF POLYHALOALKANES TO UNSATURATED SYSTEMS 4. SYNTHESIS OF SUBSTITUTED FUROPYRIMIDINES

Belen'kii, L.I.,Antonov, D.M.,Dudinov, A.A.,Lubuzh, E.D.,Krayushkin, M.M.

, p. 109 - 114 (2007/10/02)

2-Amino-5-methyl-4-(2,2,2-trichloroethyl)-3-furonitrile was synthesized from 3,5,5,5-tetrachloropentan-2-one, a product of the radical addition of CCl4 to methyl vinyl ketone, according to a scheme known for α-haloketones.The product was converted via the

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