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4-iodo-1-(methoxymethyl)-1H-pyrazole is a chemical compound with the molecular formula C5H6IN2O2. It is a derivative of pyrazole, a five-membered heterocyclic compound containing three nitrogen atoms. The molecule features a 4-iodo substituent, which is an iodine atom attached to the fourth carbon position of the pyrazole ring, and a methoxymethyl group, which is a methoxy (-OCH3) group attached to a methyl (-CH3) group, connected to the first carbon position of the pyrazole ring. 4-iodo-1-(methoxymethyl)-1H-pyrazole is often used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity.

145243-92-1

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145243-92-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 145243-92-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,5,2,4 and 3 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 145243-92:
(8*1)+(7*4)+(6*5)+(5*2)+(4*4)+(3*3)+(2*9)+(1*2)=121
121 % 10 = 1
So 145243-92-1 is a valid CAS Registry Number.

145243-92-1Downstream Products

145243-92-1Relevant academic research and scientific papers

Rapid access to pyrazolo[3,4-c]pyridines via alkyne annulation: Limitations of steric control in nickel-catalyzed alkyne insertions

Heller, Stephen T.,Natarajan, Swaminathan R.

, p. 4947 - 4950 (2007)

Polyfunctionalized pyrazolo[3,4-c]pyridines were readily prepared by the annulation of alkynes with tert-butyl 4-iodopyrazolocarboximines. The reaction was found to be catalyzed by both NiBr2(PPh3) 2/Zn or PdCl2

Substituted Quinone Synthesis by Palladium-Copper Cocatalyzed Cross-Coupling of Stannylquinones with Aryl and Heteroaryl Iodides

Liebeskind, Lanny S.,Riesinger, Steven W.

, p. 408 - 413 (1993)

A general and high-yielding route to a variety of aryl- and heteroaryl-substituted quinones is now available via the palladium-copper cocatalyzed cross-coupling of stannylquinones with aryl and heteroaryl iodides.Using this technology a number of novel aromatic- and heteroaromatic-substituted quinones were produced.Mechanistic insight is presented into the various catalytic systems used.

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