22600-77-7 Usage
Uses
Used in Medical Research:
1H-Imidazol-2-ylmethylamine dihydrochloride is used as a research compound for investigating the role of histamine in physiological processes such as allergic responses, inflammation, and gastric acid secretion. Its interaction with H1 and H2 histamine receptors makes it a valuable tool in understanding these phenomena.
Used in Therapeutic Applications:
In cancer treatment, 1H-Imidazol-2-ylmethylamine dihydrochloride is used as an immunostimulant to enhance immune responses. This property is leveraged to stimulate the body's natural defenses against cancer cells.
Used in Laboratory Settings:
Due to its solubility in water and crystalline form, 1H-Imidazol-2-ylmethylamine dihydrochloride is used as a reagent in various laboratory experiments and assays, facilitating the study of histamine receptor interactions and related biological activities.
Check Digit Verification of cas no
The CAS Registry Mumber 22600-77-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,6,0 and 0 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 22600-77:
(7*2)+(6*2)+(5*6)+(4*0)+(3*0)+(2*7)+(1*7)=77
77 % 10 = 7
So 22600-77-7 is a valid CAS Registry Number.
InChI:InChI=1/C4H7N3.2ClH/c5-3-4-6-1-2-7-4;;/h1-2H,3,5H2,(H,6,7);2*1H
22600-77-7Relevant academic research and scientific papers
NMR characterization of hydrate and aldehyde forms of imidazole-2- carboxaldehyde and derivatives
Lazaro Martinez, Juan Manuel,Romasanta, Pablo Nicolas,Chattah, Ana Karina,Buldain, Graciela Yolanda
supporting information; experimental part, p. 3208 - 3213 (2010/08/19)
The existence and stability of the aldehyde-hydrate form of imidazole-2-carboxaldehyde (4) were studied using FTIR together with solution- and solid-state NMR experiments. The results allowed us to conclude that the hydrate form was stable and precipitate
Reactivities of 2-aminomethylimidazole: An approach for a synthesis of imidazo[1,5-a]imidazole
Park, Sujin,Kang, Yonghan
, p. 2393 - 2400 (2007/10/03)
A synthesis of 5-oxo-1H-5,6-dihydroimidazo[1,5-a]imidazole which has 5,5-fused heteroaromatic ring system is described.
(8,9-Dihydro-7H-imidazodiazepin-5-yl)-cyanamide und homologe Imidazo-Bizyklen
Buschauer, A.,Schunack, W.
, p. 753 - 757 (2007/10/02)
The reaction of the 2-(ω-aminoalkyl)imidazoles 4a-f with N-cyanodiphenylimidocarbonate (7) leads to appropriately hydrogenated imidazoimidazoles, imidazodiazepines and imidazodiazocines (9a-f), which are similar to (7,8-dihydroimidazopyrimidin-5-yl)cyanamides (3) in respect to their chemical and spectroscopic properties.
