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42361-45-5

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42361-45-5 Usage

General Description

2-Furancarboxamide, N-methoxy-(9CI) is an organic compound with the molecular formula C6H7NO3. It is a derivative of furan, a heterocyclic compound and is classified as a carboxamide. The N-methoxy group signifies that a methoxy (CH3O) functional group is attached to the nitrogen atom in the carboxamide moiety. 2-Furancarboxamide, N-methoxy-(9CI) may be used in organic synthesis and chemical research, although its specific applications and properties have not been extensively documented. 2-Furancarboxamide,N-methoxy-(9CI) may have potential use in pharmaceutical and medicinal chemistry due to its structural characteristics and properties as a carboxamide derivative. However, further research and studies are needed to fully understand and explore the potential applications and effects of 2-Furancarboxamide, N-methoxy-(9CI).

Check Digit Verification of cas no

The CAS Registry Mumber 42361-45-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,3,6 and 1 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 42361-45:
(7*4)+(6*2)+(5*3)+(4*6)+(3*1)+(2*4)+(1*5)=95
95 % 10 = 5
So 42361-45-5 is a valid CAS Registry Number.

42361-45-5Relevant articles and documents

Pd(II)-Catalyzed asymmetric oxidative annulation of N-alkoxyheteroaryl amides and 1,3-dienes

Zhang, Tao,Shen, Hong-Cheng,Xu, Jia-Cheng,Fan, Tao,Han, Zhi-Yong,Gong, Liu-Zhu

, p. 2048 - 2051 (2019/03/29)

The first Pd(II)-catalyzed asymmetric oxidative annulation of N-alkoxyaryl amides and 1,3-dienes is reported, which features particular applicability for quick assembly of different types of chiral heterocycles with high yields and enantioselectivities. A novel chiral pyridine-oxazoline bearing a methoxyl group at the C-5 position and a gem-dimethyl group on the oxazoline moiety was found to be crucial for conversion.

Copper-catalyzed C-N bond formation through C-H/N-H activation: A novel approach to the synthesis of multisubstituted ureas

Jiang, Honglai,Lin, Aijun,Zhu, Chengjian,Cheng, Yixiang

supporting information, p. 819 - 821 (2013/02/23)

A copper-catalyzed cross-dehydrogenative coupling reaction that involves C-H activation of formamides and N-H activation of N-alkoxy amides has been developed. This protocol affords a novel approach to the synthesis of multisubstituted ureas under mild co

Copper-catalyzed cross-coupling of O -alkyl hydroxamates with aryl iodides

Kukosha, Tatyana,Trufilkina, Nadezhda,Belyakov, Sergey,Katkevics, Martins

supporting information; experimental part, p. 2413 - 2423 (2012/09/07)

N-Aryl-O-alkylhydroxamic acid derivatives were prepared by copper-catalyzed cross-coupling of hydroxamates with aryl iodides. The reaction conditions are compatible with standard hydroxy-protecting groups on the hydroxylamine moiety and are applicable to

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