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1-methyl-2-(3-formylfuryl-2)imidazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

147591-71-7

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147591-71-7 Usage

Imidazole derivative

A class of organic compounds that have a five-membered ring structure with two non-adjacent nitrogen atoms.

Yellowish-brown crystalline solid

The physical appearance of the compound, which is a yellow to brown crystalline solid.

Structure components

A methyl group (CH3) and a furan ring with a formyl group (CHO) attached.

Use as a reagent in organic synthesis

The compound can be used as a reagent to facilitate chemical reactions in organic synthesis processes.

Pharmaceutical research applications

The compound has potential applications in the development of new drugs and materials, making it valuable for pharmaceutical research.

Valuable tool for organic chemistry investigation

The properties and reactivity of 1-methyl-2-(3-formylfuryl-2)imidazole make it a useful compound for studying and understanding organic chemistry processes.

Check Digit Verification of cas no

The CAS Registry Mumber 147591-71-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,7,5,9 and 1 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 147591-71:
(8*1)+(7*4)+(6*7)+(5*5)+(4*9)+(3*1)+(2*7)+(1*1)=157
157 % 10 = 7
So 147591-71-7 is a valid CAS Registry Number.

147591-71-7Downstream Products

147591-71-7Relevant academic research and scientific papers

2-SUBSTITUTED IMIDAZOLES. 3. METALLATION OF 1-METHYL-2-PHENYL- AND 1-METHYL-2-(FURYL-2)IMIDAZOLES

Stoyanov, V. M.,El'chaninov, M. M.,Pozharskii, A. F.

, p. 53 - 57 (2007/10/02)

1-Methyl-2-phenylimidazole reacts with butyllithium to give 5-lithium substituted products.On the other hand, 1-methyl-2-(furyl-2)imidazole is metallated under the same conditions exclusively on the furan ring and primarily in the 3 position.The introduction of triethylamine into the reaction mixture, or replacement of butyllithium by lithium 2,2,6,6-tetramethylpiperidide leads to the formation of a lithium derivative substituted at the 5-position of the furan ring exclusively.

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