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α-(Adamant-1-ylimino)-p-methoxytoluene is a complex organic compound characterized by its unique molecular structure. It features an adamantane-1-yl group, which is a rigid, cage-like structure, connected to an imino group. This imino group is in turn bonded to a p-methoxytoluene moiety, which consists of a toluene ring with a methoxy group at the para position. The compound is known for its potential applications in various fields, including pharmaceuticals and materials science, due to its specific chemical properties and reactivity. Its synthesis and study can provide insights into the behavior of such structurally intriguing molecules, which may lead to the development of new compounds with specialized functions.

54671-67-9

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54671-67-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 54671-67-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,6,7 and 1 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 54671-67:
(7*5)+(6*4)+(5*6)+(4*7)+(3*1)+(2*6)+(1*7)=139
139 % 10 = 9
So 54671-67-9 is a valid CAS Registry Number.

54671-67-9Downstream Products

54671-67-9Relevant academic research and scientific papers

α-Acyl-α-diazoacetates in Transition-Metal-Free β-Lactam Synthesis

Synofzik, Judith,Dar'In, Dmitry,Novikov, Mikhail S.,Kantin, Grigory,Bakulina, Olga,Krasavin, Mikhail

, p. 12101 - 12110 (2019)

Thermally promoted reaction of α-acyl-α-diazoacetates with imines has been investigated. The transformation, earlier reported predominantly under transition metal catalyzed conditions, delivers α-alkoxycarbonyl-substituted β-lactams with outstanding diastereoselectivity. DFT calculations performed in order to evaluate energetically feasible reaction pathways revealed the intermediacy of 1,3-oxazin-4-one intermediates hitherto never implicated in the Staudinger synthesis of β-lactams.

Preparation of N,N-difluoroamines

-

, (2008/06/13)

N,N-difluoroamines are prepared by fluorination of compounds containing a >C=N-- bond using molecular fluorine or a hypofluorite in which the fluoroxy group is bonded to an inert electron attracting group, such hypofluorites including fluoroalkyl hypofluo

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