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10070-92-5
5-Pyrimidinecarboxaldehyde

Catalog#:1P00034V

CAS:10070-92-5

MDL:MFCD03426065

Molecular Formula:C5H4N2O

Molecular Weight:108.0981

UN Number:

Haz Class:

Packing Group:

Synonyms: Pyrimidine-5-carbaldehyde; 10070-92-5; PubChem5298; pyrimidine-5-aldehyde; AC1Q6PXT; pyrimidine 5-carboxaldehyde; AC1MC40Z; KSC174K8P; SCHEMBL193843; AMMD00015; CTK0H4587; 5-Pyrimidinecarboxaldehyde, 95%; Pyrimidine-5-carboxaldehyde; DTXSID10375493; FREJAOSUHFGDBW-UHFFFAOYSA-N; ZINC154066; ACT08630; BCP26695; ANW-49694; BBL100269; CP-412; SBB065690; STL553835; 5-formylpyrimidine; AKOS005144225; AC-6955; AN-1088; CS-W007340; HP21336; PB32342; PS-9295; QC-4417; RP00452; RTC-020701; 5-PYRIMIDINECARBOXALDEHYDE; TRA0074538; KS-000002Z8; pyrimidine-5-carboxaldehyde, AldrichCPR; AJ-13143; AK-25240; BC200327; BP-10257; BR-25240; CJ-01317; HC210384; pyrimidine-5-carboxyaldehyde; SC-00049; SY002007; AB0012601; AB1001289; DB-030315; ST1141096; TC-020701; 4CH-013849; AM20070656; FT-0084555; 5-pyrimidinecarbaldehyde; FT-0603722; FT-0700997; MFCD03426065 (97%); C-1487; 070P925; I03-0133; W-200631; F8881-5907; null; C5H4N2O; MFCD03426065; ZINC00154066; ACN-026636; CID2761034; 5-pyrimidinecarboxaldehyde (7ci,8ci,9ci); pyrimidine-5-carbaldehyde, 95% - 1G 1g; C2538; A16221; 5-pyrimidinaldehyde; 5-Formyl pyrimidine;

Keywords: 10070-92-5,MFCD03426065,1P00034V,5-Pyrimidinecarboxaldehyde,C5H4N2O

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Catalog# Purity Size Price Dis. Price Availability Quantity
1P00034V 97% 250mg $9.00 $7.00 In Stock USA ADD TO CART BUY NOW
1P00034V 97% 1g $23.00 $17.00 In Stock USA ADD TO CART BUY NOW
1P00034V 97% 5g $66.00 $49.00 In Stock USA ADD TO CART BUY NOW
1P00034V 97% 10g $130.00 $97.00 In Stock USA ADD TO CART BUY NOW

  • 5-Pyrimidinecarboxaldehyde is an important building block in organic synthesis, especially in the preparation of heterocyclic compounds, which are prevalent in many pharmaceuticals, agrochemicals, and dyes. Due to the active aldehyde group attached to a pyrimidine ring, it can undergo various chemical reactions that are useful in constructing complex molecules.
    
    One of the primary applications of 5-Pyrimidinecarboxaldehyde is in the field of medicinal chemistry, where it is used to synthesize pyrimidine derivatives that demonstrate a wide range of biological activities. These derivatives are often explored for their potential use as drugs, with activities such as antiviral, antibacterial, anti-inflammatory, and anticancer effects. Because of this, 5-Pyrimidinecarboxaldehyde is frequently found as a starting material or intermediate in the synthesis of drug candidates.
    
    In addition, this compound serves as a precursor for the synthesis of ligands. Its coordinating properties make it suitable for the preparation of various metal complexes, which can have applications in catalysis. For instance, modified pyrimidine derivatives can be employed as ligands in transition metal catalysts that are used for carbon-carbon or carbon-nitrogen bond-forming reactions.
    
    Furthermore, 5-Pyrimidinecarboxaldehyde is used in Suzuki coupling reactions. In the presence of a palladium catalyst, this compound can be coupled with boronic acids or esters to form more complex biaryls, which are structures commonly found in pharmaceuticals and organic electronic materials.
    
    Finally, as an aldehyde functionalized heterocyclic compound, 5-Pyrimidinecarboxaldehyde is involved in the Knoevenagel condensation reactions to form carbon-carbon double bonds, leading to the synthesis of diverse conjugated systems which are prevalent in dye chemistry and materials science. This versatility illustrates its utility in a broad scope of synthetic applications.

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