343569-06-2 Usage
Uses
Used in Organic Synthesis:
1-Methyl-1H-imidazole-5-carbonyl chloride hydrochloride is used as a reagent in chemical reactions for its ability to introduce the imidazole-5-carbonyl chloride functional group into other molecules, facilitating the synthesis of various organic compounds.
Used in Pharmaceutical Research:
1-Methyl-1H-imidazole-5-carbonyl chloride hydrochloride is used as a key intermediate in the development of pharmaceutical drugs and other biologically active compounds, owing to its potential applications in creating novel drug candidates with unique therapeutic properties.
Used in Chemical Reactions:
In the Chemical Synthesis Industry, 1-Methyl-1H-imidazole-5-carbonyl chloride hydrochloride is used as a reagent for its reactivity in introducing the imidazole-5-carbonyl chloride group, which is crucial for the synthesis of complex organic molecules.
Used in Drug Development:
In the Pharmaceutical Industry, 1-Methyl-1H-imidazole-5-carbonyl chloride hydrochloride is used as a building block for the creation of new drug candidates, leveraging its chemical properties to enhance the development of innovative therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 343569-06-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,3,5,6 and 9 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 343569-06:
(8*3)+(7*4)+(6*3)+(5*5)+(4*6)+(3*9)+(2*0)+(1*6)=152
152 % 10 = 2
So 343569-06-2 is a valid CAS Registry Number.
InChI:InChI=1/C5H5ClN2O/c1-8-3-7-2-4(8)5(6)9/h2-3H,1H3
343569-06-2Relevant articles and documents
Synthesis of xestomanzamines a and b
Burm, Brigitte E.A.,Blokker, Peter,Jongmans, Edwin,Van Kampen, Erwin,Wanner, Martin J.,Koomen, Gerrit-Jan
, p. 495 - 503 (2007/10/03)
Synthetic pathways are described for the synthesis of two naturally occurring β-carbolines, xestomanzamine A and B. The synthesis of aromatic xestomanzamine A was most conveniently achieved by way of a Grignard reaction in dichloromethane. This route is suitable for the synthesis of analogues with modifications in the imidazole ring of xestomanzamine A. Xestomanzamine B, an oxidation-sensitive dihydro-β-carboline, was prepared by Pictet-Spengler condensation of tryptamine with a vicinal tricarbonyl substituted imidazole.
