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Imidazole-2-carboxaldehyde

CAS No.
10111-08-7
Chemical Name:
Imidazole-2-carboxaldehyde
Synonyms
1H-IMIDAZOLE-2-CARBALDEHYDE;2-imidazolecarbaldehyde;2-IMIDAZOLECARBOXALDEHYDE;IMIDAZOLE-2-CARBALDEHYDE;2-FORMYLIMIDAZOLE;1H-IMIDAZOLE-2-CARBOXALDEHYDE;1H-iMidazol-2-carbaldehyde;JACS-10111-08-7;2-AcetliMidazole;2-FORMAYLIMIDAZOLE
CBNumber:
CB0289520
Molecular Formula:
C4H4N2O
Molecular Weight:
96.09
MDL Number:
MFCD00003544
MOL File:
10111-08-7.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-05-27 17:34:50

Imidazole-2-carboxaldehyde Properties

Melting point 209 °C (dec.) (lit.)
Boiling point 296.5±23.0 °C(Predicted)
Density 1.322±0.06 g/cm3(Predicted)
storage temp. Keep in dark place,Inert atmosphere,Room temperature
solubility DMSO (Sparingly), Methanol (Slightly, Sonicated)
form Solid
pka 11.48±0.10(Predicted)
color Light Brown to Brown
Water Solubility Soluble in water.
Sensitive Air Sensitive
BRN 4371302
InChI InChI=1S/C4H4N2O/c7-3-4-5-1-2-6-4/h1-3H,(H,5,6)
InChIKey XYHKNCXZYYTLRG-UHFFFAOYSA-N
SMILES C1(C=O)NC=CN=1
CAS DataBase Reference 10111-08-7(CAS DataBase Reference)
NIST Chemistry Reference 1H-imidazole-2-carboxaldehyde(10111-08-7)
UNSPSC Code 12352005
NACRES NA.22

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P261-P264-P271-P280-P302+P352-P305+P351+P338
target organs Respiratory system
PPE dust mask type N95 (US), Eyeshields, Gloves
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  26-36-36/37/39-3
WGK Germany  3
10
HazardClass  IRRITANT
HS Code  29332900
Storage Class 11 - Combustible Solids
Hazard Classifications Eye Irrit. 2
Skin Irrit. 2
STOT SE 3
NFPA 704
1
2 0

Imidazole-2-carboxaldehyde price More Price(101)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 272000 2-Imidazolecarboxaldehyde 97% 10111-08-7 1g $53.6 2026-04-30 Buy
Sigma-Aldrich 272000 2-Imidazolecarboxaldehyde 97% 10111-08-7 5g $143 2026-04-30 Buy
TCI Chemical I0809 Imidazole-2-carboxaldehyde >98.0%(HPLC)(T) 10111-08-7 1g $32 2026-04-30 Buy
TCI Chemical I0809 Imidazole-2-carboxaldehyde >98.0%(HPLC)(T) 10111-08-7 5g $101 2026-04-30 Buy
Usbiological 280314 Imidazole-2-carboxaldehyde Asreported 10111-08-7 50g $842 2026-06-03 Buy
Product number Packaging Price Buy
272000 1g $53.6 Buy
272000 5g $143 Buy
I0809 1g $32 Buy
I0809 5g $101 Buy
280314 50g $842 Buy

Imidazole-2-carboxaldehyde Chemical Properties,Uses,Production

Chemical Properties

White to light brown solid

Uses

1H-Imidazole-2-carboxaldehyde is a novel PTP1b inhibitor with potential application to treat type 2 diabetes.

Uses

Imidazole-2-carboxaldehyde is a novel protein tyrosine phosphatase 1B (PTP1B) inhibitor with an important application to treat type-2 diabetes. It is used in the preparation of tridentate Schiff-base carboxylate-containing ligands by undergoing condensation reaction with amino acids beta-alanine and 2-aminobenzoic acid. It is also involved in the study of the imidazole-directed allylation of aldimines.

Uses

Used in a study of the imidazole-directed allylation of aldimines.1

Synthesis Reference(s)

Organic Syntheses, Coll. Vol. 7, p. 287, 1990
The Journal of Organic Chemistry, 60, p. 1090, 1995 DOI: 10.1021/jo00109a052

Synthesis

2-Bromo-1H-imidazole

16681-56-4

N,N-Dimethylformamide

68-12-2

Imidazole-2-carboxaldehyde

10111-08-7

To a solution of 2-bromo-1H-imidazole (0.65 g, 4.4 mmol, 1.0 eq.) in anhydrous THF (20 mL) was slowly added a solution of 2 M i-PrMgCl in THF (2.2 mL, 4.4 mmol, 1.0 eq.) over 5 min at 0 °C. The reaction mixture was continued to be stirred at this temperature for 5 min. Subsequently, a hexane solution of 2.5 M n-BuLi (3.5 mL, 8.8 mmol, 2.0 eq.) was added dropwise over 5 min while the reaction temperature was controlled below 20 °C. After dropwise addition, the reaction mixture was stirred at this temperature for 30 min. Then, dry N,N-dimethylformamide (DMF, 0.32 g, 4.4 mmol, 1.0 eq.) was added and the reaction mixture was slowly warmed up to 20 °C over 0.5 h. The reaction was completed with the addition of 6 mL of N,N-dimethylformamide. Upon completion of the reaction, the reaction was quenched with 6 mL of water, kept below 20 °C and stirred for 10 min. The organic and aqueous phases were separated and the aqueous phase was extracted once with ethyl acetate (10 mL). The organic phases were combined, and the resulting suspension was returned to room temperature, filtered through a silica gel pad (0.5 cm × 1 cm), and eluted with 10 mL of ethyl acetate. The filtrate was concentrated and the residue was purified by rapid chromatography on silica gel (eluent: petroleum ether/ethyl acetate = 10:1) to afford 2-imidazolecarboxaldehyde (3k) as a light yellow solid with a yield of 0.38 g (91% yield) and a melting point of 205-206 °C. 1H-NMR (600 MHz, DMSO-d6) δ 13.60 (s, 1H), 9.64 (s, 1H) , 7.42 (s, 2H).13C-NMR (151 MHz, DMSO-d6) δ 181.66, 146.09.

References

[1] Molecules, 2017, vol. 22, # 11,

67478-50-6
10111-08-7
Synthesis of Imidazole-2-carboxaldehyde from 1-Tritylimidazole-2-carboxaldehyde
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View Lastest Price from Imidazole-2-carboxaldehyde manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Imidazole-2-carboxaldehyde pictures 2026-05-28 Imidazole-2-carboxaldehyde
10111-08-7
$2.00-5.00 1KG 99% 10000kg Hebei Chuanghai Biotechnology Co,.LTD
Imidazole-2-carboxaldehyde pictures 2025-05-26 Imidazole-2-carboxaldehyde
10111-08-7
$3.00 1kg 0.99 1000 Hebei Fengjia New Material Co., Ltd
Imidazole-2-carboxaldehyde pictures 2025-04-04 Imidazole-2-carboxaldehyde
10111-08-7
1kg 98% 1Ton Henan Aochuang Chemical Co.,Ltd.
1H-IMIDAZOLE-2-CARBOXALDEHYDE 2-Formylimidazole 2-Imidazolecarboxaldehyde 2-FORMYLIMIDAZOLE IMIDAZOL-2-CARBALDEHYDE IMIDAZOLE-2-CARBOXALDEHYDE TIMTEC-BB SBB004383 2-FORMYL IMIDAZOLE (IMIDAZOLE-2-CARBOXALDEHYDE) 2-H-imidazole-1-carboxaldehyde 2-FORMAYLIMIDAZOLE 1H-iMidazol-2-carbaldehyde Imidazole-2-carboxaldehyde p 2-imidazolecarbaldehyde Imidazole-2-carboxaldehyde ,98% Imidazole-2-carboxal 2-AcetliMidazole 2-Formyl-1H-imidazole 2-IMidazolecarboxaldehyde 97% Imidazole-2-carboxaldehyde,97% JACS-10111-08-7 Imidazole-2-carboxaldehyde> IMIDAZOLE-2-CARBOXALDEHYDE 10111-08-7 Imidazole-2-carboxaldehyde ISO 9001:2015 REACH High purity CAS 10111-08-7 Imidazole-2-carboxaldehyde in stock 6-Amino-2,4-dichloro-18-methylphenol&hydrochloride Imidazole-2-carboxaldehyde (7CI, 8CI) imidazole-2-aldehyde Imidazole-2-formaldehyde 1H-IMIDAZOLE-2-CARBALDEHYDE 2-IMIDAZOLECARBOXALDEHYDE IMIDAZOLE-2-CARBALDEHYDE 10111-08-7 1011-08-7 ALDEHYDE Heterocyclic Building Blocks Imidazoles Building Blocks Imidazoles & Benzimidazoles Building Blocks Heterocyclic Building Blocks Imidazole Imidazol&Benzimidazole Imidaxoles Building Blocks C1 to C6 Carbonyl Compounds Chemical Synthesis Heterocyclic Building Blocks Organic Building Blocks Aldehydes blocks Imidazoles Imidazoles & Benzimidazoles