343569-06-2 Usage
General Description
1-Methyl-1H-imidazole-5-carbonyl chloride hydrochloride is a chemical compound that is used in organic synthesis and pharmaceutical research. It is a derivative of imidazole, an important heterocyclic compound. The carbonyl chloride group in the molecule makes it a reactive intermediate that can be used in the production of various organic compounds. The hydrochloride salt form of this compound makes it more stable and easier to handle in laboratory settings. It is commonly used as a reagent in chemical reactions to introduce the imidazole-5-carbonyl chloride functional group into other molecules, and it has potential applications in the development of pharmaceutical drugs and other biologically active compounds. Overall, 1-Methyl-1H-imidazole-5-carbonyl chloride hydrochloride is a versatile chemical building block with a range of potential uses in the field of chemistry and drug development.
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.
