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(4-Hydroxy-2,6-Dimethyl-pyrimidin-5-yl)-acetic acid is a pyrimidine derivative, a class of organic compounds known for their six-membered ring containing nitrogen atoms. This specific compound is distinguished by the presence of hydroxy, methyl, and acetic acid functional groups attached to the pyrimidine ring. The structural configuration of this chemical suggests its potential for diverse interactions and roles in various biological activities. The properties and applications of (4-HYDROXY-2,6-DIMETHYL-PYRIMIDIN-5-YL)-ACETIC ACID can be influenced by factors such as temperature and pressure, which are common for most chemicals. Further research and experimentation are necessary to explore its potential uses in different fields.

5536-40-3

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5536-40-3 Usage

Uses

Used in Pharmaceutical Industry:
(4-Hydroxy-2,6-Dimethyl-pyrimidin-5-yl)-acetic acid is used as a chemical intermediate for the synthesis of various pharmaceutical compounds. Its unique structure allows it to be a key component in the development of new drugs, particularly those targeting specific biological pathways or receptors.
Used in Chemical Research:
In the field of chemical research, (4-Hydroxy-2,6-Dimethyl-pyrimidin-5-yl)-acetic acid serves as a valuable compound for studying the effects of different functional groups on the properties and reactivity of pyrimidine derivatives. This can lead to a better understanding of the underlying chemistry and potential applications in various industries.
Used in Material Science:
(4-Hydroxy-2,6-Dimethyl-pyrimidin-5-yl)-acetic acid may be utilized in the development of new materials with specific properties, such as improved stability or reactivity. Its incorporation into polymers or other materials could result in novel applications in areas like electronics, coatings, or adhesives.
Used in Agricultural Industry:
As a chemical compound with potential biological activity, (4-Hydroxy-2,6-Dimethyl-pyrimidin-5-yl)-acetic acid could be explored for its possible use in the agricultural industry. It may have applications as a pesticide, herbicide, or growth regulator, depending on its effects on plants and pests. Further research would be required to determine its safety and efficacy in this context.

Check Digit Verification of cas no

The CAS Registry Mumber 5536-40-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,3 and 6 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5536-40:
(6*5)+(5*5)+(4*3)+(3*6)+(2*4)+(1*0)=93
93 % 10 = 3
So 5536-40-3 is a valid CAS Registry Number.
InChI:InChI=1/C8H10N2O3/c1-4-6(3-7(11)12)8(13)10-5(2)9-4/h3H2,1-2H3,(H,11,12)(H,9,10,13)

5536-40-3 Well-known Company Product Price

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  • Aldrich

  • (CBR00564)  (4-Hydroxy-2,6-dimethylpyrimidin-5-yl)acetic acid  AldrichCPR

  • 5536-40-3

  • CBR00564-1G

  • 966.42CNY

  • Detail

5536-40-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-Hydroxy-2,6-dimethyl-pyrimidin-5-yl)-acetic acid

1.2 Other means of identification

Product number -
Other names 2-(2,6-dimethyl-4-oxo-1H-pyrimidin-5-yl)acetic acid

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:5536-40-3 SDS

5536-40-3Downstream Products

5536-40-3Relevant academic research and scientific papers

Dimethyl acetylsuccinate as a versatile synthon in heterocyclic chemistry - A facile synthesis of heterocyclic acetic acid derivatives

Craig, G. Wayne,Eberle, Martin,Lamberth, Clemens,Vettiger, Thomas

, p. 504 - 507 (2007/10/03)

The preparation of novel acetic acid derivatives of pyrazole 3a,b and pyrimidine 2a-e is achieved by condensation of dimethyl acetylsuccinate (1) with appropriate reaction partners. Also triethyl 1,1,2-ethanetricarboxylate (6) is a valuable starting material, which is demonstrated by the synthesis of previously unknown pyrimidin-5-yl acetates. Wiley-VCH Verlag GmbH, 2000.

Pyrimidinyl acrylic acid derivatives

-

, (2008/06/13)

The invention discloses compounds of formula I It has now been found that compounds of formula I STR1 wherein R1 is hydrogen, methyl, ethyl or trifluoromethyl, and R2 is hydrogen, methyl, ethyl, C1-4 alkylthio, C1-4/

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