Basic information Safety Supplier Related

1-Methyl-1H-imidazole-2-carboxylic acid

Basic information Safety Supplier Related

1-Methyl-1H-imidazole-2-carboxylic acid Basic information

Product Name:
1-Methyl-1H-imidazole-2-carboxylic acid
Synonyms:
  • 1-METHYL-1H-IMIDAZOLE-2-CARBOXYLIC ACID >98%
  • 1-Methyl-1H-imidazole-2-carboxylic acid lithiumsalt
  • CHEMBRDG-BB 4401397
  • IFLAB-BB F2124-0530
  • RARECHEM AL BE 0638
  • 1-Methyl-1h-imidazole-2-carboxylic acid, tech
  • 1-Methylimidazole-2-carboxylic acid hydrate, 90+%
  • 1-Methyl-1H-imidazole-2-carboxylic acid ,97%
CAS:
20485-43-2
MF:
C5H6N2O2
MW:
126.11
EINECS:
626-320-6
Product Categories:
  • Heterocycles
  • Building Blocks
  • Heterocyclic Building Blocks
  • Imidazol&Benzimidazole
  • Miscellaneous Reagents
  • blocks
  • Carboxes
  • Imidazoles
Mol File:
20485-43-2.mol
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1-Methyl-1H-imidazole-2-carboxylic acid Chemical Properties

Melting point:
104 °C (dec.)
Boiling point:
339.4±25.0 °C(Predicted)
Density 
1.34±0.1 g/cm3(Predicted)
storage temp. 
Sealed in dry,Store in freezer, under -20°C
solubility 
Methanol (Slightly), Water (Slightly)
form 
Solid
pka
1.24±0.31(Predicted)
color 
White to Off-White
Sensitive 
Hygroscopic
Stability:
Temperature Sensitive
InChI
InChI=1S/C5H6N2O2/c1-7-3-2-6-4(7)5(8)9/h2-3H,1H3,(H,8,9)
InChIKey
WLDPWZQYAVZTTP-UHFFFAOYSA-N
SMILES
C1(C(O)=O)N(C)C=CN=1
CAS DataBase Reference
20485-43-2(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36/37/39-37/39-36
WGK Germany 
3
Hazard Note 
Irritant
HS Code 
29332900
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1-Methyl-1H-imidazole-2-carboxylic acid Usage And Synthesis

Chemical Properties

White Crystalline Solid

Uses

It is useful for solid phase synthesis of polyamides containing imidazole.

Uses

1-Methyl-1H-imidazole-2-carboxylic acid is a useful synthetic intermediate for solid phase synthesis of polyamides containing imidazole

Definition

ChEBI: 1-methyl-imidazole-2-carboxylic acid is an imidazolyl carboxylic acid that is 1H-imidazole with methyl and carboxylic acid group substituents at positions 1 and 2 respectively. It has a role as a metabolite.

Synthesis

13750-81-7

20485-43-2

The general procedure for the synthesis of 1-methyl-1H-imidazole-2-carboxylic acid from 1-methyl-1H-imidazole-2-carboxaldehyde is as follows: first, 1-methyl-1H-imidazole-2-carboxaldehyde was prepared by referring to the method described in literature [23]. Subsequently, the synthetic procedure for Im2COOH (1b) was followed, and the reaction yield was up to quantitative levels after removal of water under high vacuum (without diethyl ether/water washing). Note that heating may cause decarboxylation to occur. Product yield: 100%. Melting point range is 99-101 °C. NMR hydrogen spectrum (400MHz, D2O): δH 7.42, 7.39 (2H, single peak, imidazolium cyclic-H), 4.08 ppm (3H, single peak, N-CH3); NMR carbon spectrum (400MHz, D2O): δC 158.67, 139.68, 125.83, 118.46, 36.73 ppm. infrared spectrum ( KBr press method): ν 3347 (medium intensity), 3119 (medium intensity), 2663 (weak), 1641 (strong), 1683 (medium intensity), 1507 (strong), 1449 (medium intensity), 1388 (strong), 1338 (strong), 1285 (strong), 1173 (medium intensity), 1123 (strong), 961 (medium intensity), 910 (medium), 776 (strong), 685 (strong) cm-1. Calculated values from elemental analysis (C5H8N2O3, molecular weight 144.12): C, 41.67%; H, 5.59%; N, 19.44%. Measured values: C, 41.28%; H, 5.23%; N, 19.12%.

References

[1] South African Journal of Chemistry, 2010, vol. 63, p. 95 - 104
[2] Journal of Inorganic Biochemistry, 2015, vol. 145, p. 11 - 18
[3] South African Journal of Chemistry, 2012, vol. 65, p. 231 - 238

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