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N-(adamantan-2-yl)cyclohexanecarboxamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

325820-49-3

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325820-49-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 325820-49-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,5,8,2 and 0 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 325820-49:
(8*3)+(7*2)+(6*5)+(5*8)+(4*2)+(3*0)+(2*4)+(1*9)=133
133 % 10 = 3
So 325820-49-3 is a valid CAS Registry Number.

325820-49-3Downstream Products

325820-49-3Relevant academic research and scientific papers

Novel 11β-HSD1 inhibitors: C-1 versus C-2 substitution and effect of the introduction of an oxygen atom in the adamantane scaffold

Leiva, Rosana,Seira, Constantí,McBride, Andrew,Binnie, Margaret,Luque, F. Javier,Bidon-Chanal, Axel,Webster, Scott P.,Vázquez, Santiago

, p. 4250 - 4253 (2015)

The adamantane scaffold is found in several marketed drugs and in many investigational 11β-HSD1 inhibitors. Interestingly, all the clinically approved adamantane derivatives are C-1 substituted. We demonstrate that, in a series of paired adamantane isomer

Photoinduced, copper-catalyzed alkylation of amides with unactivated secondary alkyl halides at room temperature

Do, Hien-Quang,Bachman, Shoshana,Bissember, Alex C.,Peters, Jonas C.,Fu, Gregory C.

supporting information, p. 2162 - 2167 (2014/03/21)

The development of a mild and general method for the alkylation of amides with relatively unreactive alkyl halides (i.e., poor substrates for S N2 reactions) is an ongoing challenge in organic synthesis. We describe herein a versatile transition-metal-catalyzed approach: in particular, a photoinduced, copper-catalyzed monoalkylation of primary amides. A broad array of alkyl and aryl amides (as well as a lactam and a 2-oxazolidinone) couple with unactivated secondary (and hindered primary) alkyl bromides and iodides using a single set of comparatively simple and mild conditions: inexpensive CuI as the catalyst, no separate added ligand, and C-N bond formation at room temperature. The method is compatible with a variety of functional groups, such as an olefin, a carbamate, a thiophene, and a pyridine, and it has been applied to the synthesis of an opioid receptor antagonist. A range of mechanistic observations, including reactivity and stereochemical studies, are consistent with a coupling pathway that includes photoexcitation of a copper-amidate complex, followed by electron transfer to form an alkyl radical.

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