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4-Pyrimidinecarboxylic acid

CAS No.
31462-59-6
Chemical Name:
4-Pyrimidinecarboxylic acid
Synonyms
PYRIMIDINE-4-CARBOXYLIC ACID;4-Pyrimidinecarboxylicaci;4-PYRIMIDINECARBOXYLIC ACID;Pyrimidine-4-carboxylic a...;Pyrimidin-4-yl-carboxylic acid;Pyrimidine-4-carboxylic acid ,98%;4-Pyrimidinecarboxylic acid (6CI,8CI,9CI);4-Carboxypyrimidine, 4-Carboxy-1,3-diazine;4-Pyrimidinecarboxylic acid ISO 9001:2015 REACH;4-PYRIMIDINECARBOXYLIC ACID,PYRIMIDINE-4-CARBOXYLIC ACID
CBNumber:
CB6766207
Molecular Formula:
C5H4N2O2
Molecular Weight:
124.1
MDL Number:
MFCD00129737
MOL File:
31462-59-6.mol
MSDS File:
SDS
Last updated:2026-01-13 11:24:25
Product description Number Pack Size Price
4-Pyrimidinecarboxylic acid 730831 500mg $110
Pyrimidine-4-carboxylic Acid >98.0%(GC)(T) P1993 200mg $128
Pyrimidine-4-Carboxylic Acid >98% 10010564 50mg $21
Pyrimidine-4-Carboxylic Acid >98% 10010564 100mg $39
Pyrimidine-4-Carboxylic Acid >98% 10010564 250mg $82
More product size

4-Pyrimidinecarboxylic acid Properties

Melting point 229.8-231.9°C
Boiling point 318.7±15.0 °C(Predicted)
Density 1.403±0.06 g/cm3(Predicted)
storage temp. Keep in dark place,Sealed in dry,Room Temperature
solubility DMF: 5 mg/ml; DMSO: 20 mg/ml; Ethanol: 0.25 mg/ml; PBS (pH 7.2): 1 mg/ml
form powder to crystal
pka 2.81±0.10(Predicted)
color White to Light yellow
InChI InChI=1S/C5H4N2O2/c8-5(9)4-1-2-6-3-7-4/h1-3H,(H,8,9)
InChIKey YPOXGDJGKBXRFP-UHFFFAOYSA-N
SMILES C1=NC=CC(C(O)=O)=N1
CAS DataBase Reference 31462-59-6(CAS DataBase Reference)
EPA Substance Registry System 4-Pyrimidinecarboxylic acid (31462-59-6)
UNSPSC Code 12352100
NACRES NA.22

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H319
Precautionary statements  P305+P351+P338
Hazard Codes  Xi,Xn
Risk Statements  36
Safety Statements  26
WGK Germany  3
TSCA  TSCA listed
HazardClass  IRRITANT
HS Code  29339900
Storage Class 11 - Combustible Solids
Hazard Classifications Eye Irrit. 2
NFPA 704
0
2 0

4-Pyrimidinecarboxylic acid price More Price(31)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 730831 4-Pyrimidinecarboxylic acid 31462-59-6 500mg $110 2025-07-31 Buy
TCI Chemical P1993 Pyrimidine-4-carboxylic Acid >98.0%(GC)(T) 31462-59-6 200mg $128 2024-03-01 Buy
Cayman Chemical 10010564 Pyrimidine-4-Carboxylic Acid >98% 31462-59-6 50mg $21 2024-03-01 Buy
Cayman Chemical 10010564 Pyrimidine-4-Carboxylic Acid >98% 31462-59-6 100mg $39 2024-03-01 Buy
Cayman Chemical 10010564 Pyrimidine-4-Carboxylic Acid >98% 31462-59-6 250mg $82 2024-03-01 Buy
Product number Packaging Price Buy
730831 500mg $110 Buy
P1993 200mg $128 Buy
10010564 50mg $21 Buy
10010564 100mg $39 Buy
10010564 250mg $82 Buy

4-Pyrimidinecarboxylic acid Chemical Properties,Uses,Production

Chemical Properties

white solid

Uses

4-?Pyrimidinecarboxylic Acid is a reactant in copper-catalyzed heteroaryl carboxamide-directed ortho-amination of anilines with cyclic alkylamines.

Synthesis

4-Methylpyrimidine

3438-46-8

4-Pyrimidinecarboxylic acid

31462-59-6

1. Oxidation reaction: Selenium dioxide (8.82 g, 0.079 mol) was slowly added to a stirred solution of 4-methylpyrimidine (5.0 g, 0.053 mol) in pyridine (55 mL) at room temperature. The reaction mixture was stirred at 55°C for 2 hours, then warmed to 80°C and continued stirring for 3.5 hours. After completion of the reaction, it was cooled to room temperature and stirred overnight, the reaction mixture was filtered and the residue was washed with pyridine. The pyridine solution was combined and concentrated, and the resulting pyrimidine-4-carboxylic acid was washed with water to remove traces of selenium dioxide. Yield: 5.3 g, 80.5% yield. 2. Esterification reaction: Concentrated pyrimidine-4-carboxylic acid (5.0 g, 0.04 mol) was dissolved in methanol (170 mL) and hydrochloric acid (2 mL, room temperature) was added. After refluxing overnight, the reaction mixture was cooled to room temperature, neutralized with 10% sodium bicarbonate solution and concentrated. The esterified product was extracted with ether, dried over anhydrous sodium sulfate and concentrated to give methyl pyrimidine-4-carboxylate as a yellow solid. Yield: 3.3 g, yield 57.55%. 3. Amidation reaction: Trimethylacetyl chloride (11.30g, 0.093mol) was added dropwise to a solution of triethylamine (15.75g, 0.155mol) and 4-chloroaniline (10.0g, 0.078mol) in benzene (500mL) at 0℃. The reaction mixture was gradually warmed to room temperature and stirred for 3 hours. Upon completion of the reaction, it was quenched with water, extracted with ethyl acetate, washed sequentially with water and brine, and dried over anhydrous sodium sulfate. The resulting solid product was recrystallized from petroleum ether. Yield: 14.0 g, 84.43% yield. 4. Lithiation reaction: To a solution of N-(4-chlorophenyl)-2,2-dimethylpropanamide (3.5 g, 0.0165 mol) in tetrahydrofuran (50 mL) was added a hexane solution of n-butyllithium (2.64 g, 1.2 M, 0.041 mol) at 0 °C. The reaction was followed by stirring for 2 hours. After stirring at 0 °C for 2 h, the reaction was cooled to -70 °C and a tetrahydrofuran (25 mL) solution of methyl pyrimidine-4-carboxylate (3.18 g, 0.023 mol) was slowly added. The reaction mixture was then warmed to room temperature and stirred overnight. Ether (50 mL) and water (50 mL) were added and the organic layer was separated. The aqueous layer was further extracted with ether and the organic layers were combined, washed sequentially with water and brine and dried over anhydrous sodium sulfate. After concentration, the product was purified by column chromatography. Yield: 1.7 g, yield 32.69%. 5. Deprotection reaction: 70% sulfuric acid solution (10 mL) of protected aminoketone (1.7 g, 0.0054 mol) was heated at 95 °C overnight. After cooling to room temperature, it was alkalized with 10% sodium hydroxide solution, extracted with dichloromethane, washed sequentially with water and brine, and dried over anhydrous sodium sulfate. After concentration, the product was purified by basic alumina column chromatography to obtain the target compound. Yield: 0.20 g, 16% yield.

References

[1] Patent: WO2004/46092, 2004, A2. Location in patent: Page 52-53
[2] Patent: WO2008/23239, 2008, A1. Location in patent: Page/Page column 21
[3] Heterocycles, 2003, vol. 60, # 4, p. 953 - 957
[4] PLoS ONE, 2016, vol. 11, # 5,
[5] Patent: WO2008/70150, 2008, A1. Location in patent: Page/Page column 59

3438-46-8
31462-59-6
Synthesis of 4-Pyrimidinecarboxylic acid from 4-Methylpyrimidine
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View Lastest Price from 4-Pyrimidinecarboxylic acid manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
 4-Pyrimidinecarboxylic acid pictures 2019-07-06 4-Pyrimidinecarboxylic acid
31462-59-6
US $8.00 / kg 1kg 99% 10TON Career Henan Chemical Co

4-Pyrimidinecarboxylic acid Spectrum

4-PYRIMIDINECARBOXYLIC ACID 4-Pyrimidinecarboxylic acid (6CI,8CI,9CI) Pyrimidin-4-yl-carboxylic acid 4-PYRIMIDINECARBOXYLIC ACID,PYRIMIDINE-4-CARBOXYLIC ACID Pyrimidine-4-carboxylic acid ,98% Pyrimidine-4-carboxylic a... 4-Carboxypyrimidine, 4-Carboxy-1,3-diazine 4-Pyrimidinecarboxylicaci 4-Pyrimidinecarboxylic acid ISO 9001:2015 REACH PYRIMIDINE-4-CARBOXYLIC ACID 31462-59-6 250-641-7 Heterocycle-Pyrimidine series Building Blocks Carboxy Carboxylic Acids Pyrazines, Pyrimidines & Pyridazines pharmacetical Carboxylic Acids Pyrazines, Pyrimidines & Pyridazines Pyrimidine series PYRIMIDINE