754219-01-7 Usage
Description
Ethyl 5-iodo-1-methyl-1H-pyrazole-4-carboxylate is a chemical compound with the molecular formula C8H10IN3O2. It is a derivative of pyrazole, a five-membered heterocyclic compound, featuring an ethyl ester group, an iodine atom, and a methyl substituent attached to the pyrazole ring. Ethyl 5-iodo-1-methyl-1H-pyrazole-4-carboxylate is recognized for its role in organic synthesis and medicinal chemistry, where it serves as a building block for the preparation of various pharmaceutical compounds. The presence of the iodine atom allows for further functionalization, rendering it a valuable intermediate for the synthesis of a broad spectrum of organic molecules. The methyl and carboxylate groups enhance the compound's reactivity and solubility in organic solvents.
Uses
Used in Organic Synthesis:
Ethyl 5-iodo-1-methyl-1H-pyrazole-4-carboxylate is used as a key intermediate for the synthesis of a wide range of organic molecules. Its unique structure, including the iodine atom, makes it a versatile building block that can be further functionalized to create diverse organic compounds.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, Ethyl 5-iodo-1-methyl-1H-pyrazole-4-carboxylate is utilized as a precursor in the preparation of pharmaceutical compounds. Its structural features contribute to the development of new drugs with potential therapeutic applications.
Used in Pharmaceutical Industry:
Ethyl 5-iodo-1-methyl-1H-pyrazole-4-carboxylate is used as a chemical intermediate for the production of various pharmaceuticals. Its reactivity and solubility properties make it suitable for use in the synthesis of drugs that target a range of medical conditions.
Used in Research and Development:
Ethyl 5-iodo-1-methyl-1H-pyrazole-4-carboxylate is also employed in research and development settings, where it aids scientists in exploring new chemical reactions and pathways, potentially leading to the discovery of novel pharmaceutical agents and materials.
Check Digit Verification of cas no
The CAS Registry Mumber 754219-01-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,5,4,2,1 and 9 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 754219-01:
(8*7)+(7*5)+(6*4)+(5*2)+(4*1)+(3*9)+(2*0)+(1*1)=157
157 % 10 = 7
So 754219-01-7 is a valid CAS Registry Number.
754219-01-7Relevant articles and documents
AZOLE-FUSED PYRIDAZIN-3(2H)-ONE DERIVATIVES
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, (2021/04/01)
Disclosed are compounds of Formula (1) and pharmaceutically acceptable salts thereof, wherein α, β, n, R4, R5, R6, R8, R9, R10, R11, X1, X2, X3 and X7 are defined in the specification. This disclosure also relates to materials and methods for preparing compounds of Formula (1), to pharmaceutical compositions comprising them, and to their use for treating diseases, disorders, and conditions associated with GPR139.
Pd/C-mediated synthesis of α-pyrone fused with a five-membered nitrogen heteroaryl ring: A new route to pyrano[4,3-c]pyrazol-4(1H)-ones
Gorja, Dhilli Rao,Batchu, Venkateswara Rao,Ettam, Ashok,Pal, Manojit
scheme or table, (2010/04/22)
Pd/C-mediated alkynylation of 5-iodo-pyrazole-4-carboxylic acid, involving the first regioselective construction of α-pyrone ring on a pyrazol moiety via tandem coupling-cyclization process, has been developed to afford pyrano[4,3-c]pyrazol-4(1H)-one in a
