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2,4-DIHYDROXY-6-AMINO-5-DIETHOXYETHYLPYRIMIDINE, with the chemical name 2,4-Dihydroxy-6-amino-5-diethoxyethylpyrimidine (CAS# 102879-75-4), is a synthetic organic compound characterized by its pink to brown solid appearance. It is known for its utility in various organic synthesis processes, making it a valuable component in the development of new chemical entities and materials.

102879-75-4

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102879-75-4 Usage

Uses

Used in Organic Synthesis:
2,4-DIHYDROXY-6-AMINO-5-DIETHOXYETHYLPYRIMIDINE is used as a synthetic intermediate for the development of various organic compounds. Its unique structure, featuring both hydroxyl and amino groups along with a diethoxyethyl side chain, allows it to participate in a wide range of chemical reactions, facilitating the creation of new molecules with potential applications across different industries.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, 2,4-DIHYDROXY-6-AMINO-5-DIETHOXYETHYLPYRIMIDINE serves as a key building block in the synthesis of novel drug candidates. Its ability to form diverse chemical linkages makes it suitable for the design of molecules with specific therapeutic targets, potentially leading to the discovery of new treatments for various diseases and medical conditions.
Used in Chemical Research:
2,4-DIHYDROXY-6-AMINO-5-DIETHOXYETHYLPYRIMIDINE is also utilized in academic and industrial research settings as a subject of study for understanding the fundamental properties of organic compounds. Its reactivity and structural features provide insights into the mechanisms of chemical reactions and the development of innovative synthetic methodologies.
While the specific applications and industries for 2,4-DIHYDROXY-6-AMINO-5-DIETHOXYETHYLPYRIMIDINE are not explicitly detailed in the provided materials, its role as a compound useful in organic synthesis suggests a broad range of potential uses across various fields that involve the creation and manipulation of organic molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 102879-75-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,8,7 and 9 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 102879-75:
(8*1)+(7*0)+(6*2)+(5*8)+(4*7)+(3*9)+(2*7)+(1*5)=134
134 % 10 = 4
So 102879-75-4 is a valid CAS Registry Number.

102879-75-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-amino-5-(2,2-diethoxyethyl)-1H-pyrimidine-2,4-dione

1.2 Other means of identification

Product number -
Other names 2,4-DIHYDROXY-6-AMINO-5-DIETHOXYETHYLPYRIMIDINE

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:102879-75-4 SDS

102879-75-4Relevant academic research and scientific papers

PYRROLOPYRIMIDINE DERIVATIVES USED AS HSP90 INHIBITORS

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Page/Page column 37-38, (2008/06/13)

Compounds of formula (I) have HSP90 inhibitory activity and are therefore useful in the treatment of, inter alia, cancer: Formula (I) wherein Ri is hydrogen, fluoro, chloro, bromo, or a radical of formula -X-Alk1-(Z)m-(Alk2)n-Q wherein X is -O-, -S- -S(O)-, -SO2-, or -NH-, Z is -O-, -S-, -(C=O)-, -(C=S)-, -S(O)-, -SO2-, -NRA-, or, in either orientation -C(=O)O-, -C(=O)NRA- , -C(=S)NRA-, -SO2NRA-, -NRAC(=O)-, or -NRASO2- wherein RA is hydrogen or C1-C6 alkyl AIk1 and AIk2 are optionally substituted divalent C1-C3 alkylene or C2-C3 alkenylene radicals, m, n and p are independently 0 or 1 , and Q is hydrogen or an optionally substituted carbocyclic or heterocyclic radical; R2 is a radical of formula -(Ar1)p-(Alk1)q-(Z)r-(Alk2)s-Q wherein Ar1 is an optionally substituted aryl or heteroaryl radical, Alk1, Alk2, Z, and Q are as defined above, and p, q, r and s are independently 0 or 1 ; and R3 is cyano (-CN), fluoro, chloro, bromo, methyl in which in which one or more hydrogen atoms are optionally replaced by fluorine atoms, ethyl in which in which one or more hydrogen atoms are optionally replaced by fluorine atoms, cyclopropyl, -OH, -CH2OH, -C(O)NH2, -C(O)CH3, Or -NH2.

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