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N-Cyclohexyl-3,3-dimethylbutanamide is a chemical compound with the molecular formula C13H25NO. It is a white crystalline solid that is soluble in organic solvents and has a melting point of approximately 70-72°C. N-cyclohexyl-3,3-dimethylbutanamide is primarily used as a synthetic intermediate in the production of various pharmaceuticals and agrochemicals, particularly as a precursor for the synthesis of certain pesticides and drugs. Its structure consists of a cyclohexyl group attached to a 3,3-dimethylbutanamide moiety, which contributes to its unique chemical properties and reactivity. Due to its potential applications in the synthesis of various compounds, N-cyclohexyl-3,3-dimethylbutanamide is an important compound in the field of organic chemistry and pharmaceutical research.

7473-22-5

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7473-22-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7473-22-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,7 and 3 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 7473-22:
(6*7)+(5*4)+(4*7)+(3*3)+(2*2)+(1*2)=105
105 % 10 = 5
So 7473-22-5 is a valid CAS Registry Number.

7473-22-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N-cyclohexyl-3,3-dimethylbutanamide

1.2 Other means of identification

Product number -
Other names N-Cyclohexyl-3,3-dimethyl-butyramid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:7473-22-5 SDS

7473-22-5Downstream Products

7473-22-5Relevant academic research and scientific papers

Nickel-catalyzed transamidation of aliphatic amide derivatives

Dander, Jacob E.,Baker, Emma L.,Garg, Neil K.

, p. 6433 - 6438 (2017/08/29)

Transamidation, or the conversion of one amide to another, is a long-standing challenge in organic synthesis. Although notable progress has been made in the transamidation of primary amides, the transamidation of secondary amides has remained underdeveloped, especially when considering aliphatic substrates. Herein, we report a two-step approach to achieve the transamidation of secondary aliphatic amides, which relies on non-precious metal catalysis. The method involves initial Boc-functionalization of secondary amide substrates to weaken the amide C-N bond. Subsequent treatment with a nickel catalyst, in the presence of an appropriate amine coupling partner, then delivers the net transamidated products. The transformation proceeds in synthetically useful yields across a range of substrates. A series of competition experiments delineate selectivity patterns that should influence future synthetic design. Moreover, the transamidation of Boc-activated secondary amide derivatives bearing epimerizable stereocenters underscores the mildness and synthetic utility of this methodology. This study provides the most general solution to the classic problem of secondary amide transamidation reported to date.

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