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3-(1H-Imidazol-4-yl)pyridine

CAS No.
51746-85-1
Chemical Name:
3-(1H-Imidazol-4-yl)pyridine
Synonyms
CPD2017;CPDD2017;Brn 0003724;4-(3-Pyridyl)imidazol;4-(3-PYRIDYL)IMIDAZOLE;3-(4-Imidazolyl)Pyridine;3-(1H-IMidazol-5-yl)pyridine;3-(1h-imidazol-4-yl)-pyridin;3-(1H-IMIDAZOL-4-YL)PYRIDINE;3-(5-Imidazolyl)pyridine 95+%
CBNumber:
CB1106750
Molecular Formula:
C8H7N3
Molecular Weight:
145.16
MDL Number:
MFCD01691712
MOL File:
51746-85-1.mol
Last updated:2025-08-08 17:45:00

3-(1H-Imidazol-4-yl)pyridine Properties

Melting point 117-118°C
Boiling point 422.4±20.0 °C(Predicted)
Density 1.214±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
solubility Ethanol, Methanol, Water
form Solid
pka 12.29±0.10(Predicted)
color Light Yellow
InChI InChI=1S/C8H7N3/c1-2-7(4-9-3-1)8-5-10-6-11-8/h1-6H,(H,10,11)
InChIKey YFOKBFRTGLSZLU-UHFFFAOYSA-N
SMILES C1=NC=CC=C1C1NC=NC=1
CAS DataBase Reference 51746-85-1(CAS DataBase Reference)
EWG's Food Scores 1

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H332-H335
Precautionary statements  P280-P305+P351+P338-P310
HazardClass  IRRITANT
HS Code  2933998090
Toxicity mouse,LD50,intraperitoneal,250mg/kg (250mg/kg),BEHAVIORAL: GENERAL ANESTHETICLUNGS, THORAX, OR RESPIRATION: OTHER CHANGESBEHAVIORAL: EXCITEMENT,Quarterly Journal of Pharmacy & Pharmacology. Vol. 12, Pg. 260, 1939.

3-(1H-Imidazol-4-yl)pyridine price More Price(14)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Matrix Scientific 032282 3-(5-Imidazolyl)pyridine 51746-85-1 250mg $144 2021-12-16 Buy
Matrix Scientific 032282 3-(5-Imidazolyl)pyridine 51746-85-1 1g $359 2021-12-16 Buy
AK Scientific 7231AB 3-(1H-Imidazol-4-yl)pyridine 51746-85-1 500mg $364 2021-12-16 Buy
SynQuest Laboratories 3H31-1-3B 3-(5-Imidazolyl)pyridine 51746-85-1 1g $637 2021-12-16 Buy
Matrix Scientific 032282 3-(5-Imidazolyl)pyridine 51746-85-1 500mg $233 2021-12-16 Buy
Product number Packaging Price Buy
032282 250mg $144 Buy
032282 1g $359 Buy
7231AB 500mg $364 Buy
3H31-1-3B 1g $637 Buy
032282 500mg $233 Buy

3-(1H-Imidazol-4-yl)pyridine Chemical Properties,Uses,Production

Chemical Properties

Light Yellow Solid

Uses

Imidazole rings are found in numberous natural compounds such as enzymes, nucleic acid, and alkaloids that play a role in biological processes.

Synthesis

5-PYRIDIN-3-YL-1H-IMIDAZOLE-2-THIOL

93103-29-8

3-(1H-Imidazol-4-yl)pyridine

51746-85-1

General procedure for the synthesis of 3-(1H-imidazol-4-yl)pyridine from the compound (CAS:93103-29-8): 3-(1H-imidazol-4-yl)-4-(pyridin-3-yl)-1H-imidazole-2(3H)-thione (1.0 wt. portion; 1.00 equiv.), which had been prepared in step 3.1, was added to a reactor, followed by the addition of deionized water (8 vols. ). Sodium nitrite (0.58 wt. portions; 1.5 eq.) was added to the reactor, the reaction mixture was cooled to 5 °C and 65% nitric acid (1.97 vol. portions; 5 eq.) was added slowly. The inner wall of the reactor was rinsed with deionized water (2 vol. parts). The reaction mixture is heated to 35°C within 1 hour and stirred at that temperature for not less than 6 hours. In some embodiments, the reaction mixture may be heated to 85°C (e.g., for 3 hours, followed by stirring for an additional 2 hours). The mixture is cooled to 15°C and sodium carbonate (2.0 wt.) (or other base, such as sodium hydroxide) is slowly added. The solution was then heated to 30°C and saturated with sodium chloride. To the aqueous layer is added isopropanol (4 v/v) and stirred for no less than 30 minutes (the temperature may be increased in some embodiments during this process, e.g. to 55/60°C). The phases are separated, sodium chloride (2 wt. portions) is added to the aqueous layer, and the extraction of the aqueous layer is repeated once with isopropanol (4 vol. portions), and once more with isopropanol (2 vol. portions) (other solvents are optional, e.g., 2-methyltetrahydrofuran). The mixture was concentrated under vacuum to 2 vol%. The purity of the product was determined by HPLC and the structure was confirmed by NMR (see Figures 9 and 10). The yield was stable between 84-92% in multiple production runs.

References

[1] Patent: WO2014/17938, 2014, A2. Location in patent: Page/Page column 66

3-(1H-Imidazol-4-yl)pyridine Preparation Products And Raw materials

Global( 93)Suppliers
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View Lastest Price from 3-(1H-Imidazol-4-yl)pyridine manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
3-(1H-Imidazol-4-yl)pyridine pictures 2021-08-12 3-(1H-Imidazol-4-yl)pyridine
51746-85-1
US $15.00-10.00 / KG 1KG 99%+ HPLC Monthly supply of 1 ton Zhuozhou Wenxi import and Export Co., Ltd
3-(1H-Imidazol-4-yl)pyridine pictures 2020-01-09 3-(1H-Imidazol-4-yl)pyridine
51746-85-1
US $3.00 / KG 1KG 98% 200KG Career Henan Chemical Co
3-(1H-Imidazol-4-yl)pyridine pictures 2020-01-09 3-(1H-Imidazol-4-yl)pyridine
51746-85-1
US $3.00 / KG 1KG 98% 200KG Career Henan Chemical Co

3-(1H-Imidazol-4-yl)pyridine Spectrum

4-(3-PYRIDYL)IMIDAZOLE 3-(1H-IMIDAZOL-4-YL)PYRIDINE 3-(1h-imidazol-4-yl)-pyridin 3-(5-Imidazolyl)pyridine 95+% 3-(1H-Imidazol-4-yl)pyridine Discontinued See: I351751 4-(3-Pyridyl)imidazol Brn 0003724 Pyridine, 3-(1H-imidazol-4-yl)- 3-(1H-IMidazol-5-yl)pyridine Pyridine, 3-(1H-imidazol-5-yl)- 3-(1H-imidazole-4-yl)pyridine CPD2017 3-(1H-IMIDAZOL-4-YL)PYRIDINE DISCONTINUED 3-(4-Imidazolyl)Pyridine CPDD2017 1,4-Benzenedicarbonitrile,2,7-dibromo- 51746-85-1 C8H7N3SHCl Heterocycles Miscellaneous Reagents