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N-tert-butyl-2-propylpentanamide is a complex organic compound with the molecular formula C11H23NO. It is a derivative of pentanamide, featuring a tert-butyl group (a type of alkyl group) attached to the nitrogen atom and a propyl group (a three-carbon alkyl chain) attached to the second carbon of the pentane backbone. N-tert-butyl-2-propylpentanamide is characterized by its unique structure, which contributes to its specific chemical properties and potential applications in various fields, such as pharmaceuticals or chemical research. Due to its specific functional groups and molecular structure, N-tert-butyl-2-propylpentanamide may exhibit unique reactivity and stability, making it a subject of interest for further study and development.

2751-06-6

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2751-06-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2751-06-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,7,5 and 1 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2751-06:
(6*2)+(5*7)+(4*5)+(3*1)+(2*0)+(1*6)=76
76 % 10 = 6
So 2751-06-6 is a valid CAS Registry Number.

2751-06-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name N-tert-butyl-2-propylpentanamide

1.2 Other means of identification

Product number -
Other names 2-Propyl-valeriansaeure-tert.-butylamid

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:2751-06-6 SDS

2751-06-6Downstream Products

2751-06-6Relevant academic research and scientific papers

Ligand-Controlled Regiodivergent Catalytic Amidation of Unactivated Secondary Alkyl Bromides

Tortajada, Andreu,Menezes Correia, Jose Tiago,Serrano, Eloisa,Monleón, Alicia,Tampieri, Alberto,Day, Craig S.,Juliá-Hernández, Francisco,Martin, Ruben

, p. 10223 - 10227 (2021/08/24)

A regiodivergent Ni-catalyzed amidation of unactivated secondary alkyl bromides is described. The site-selectivity of the amidation event is dictated by subtle differences on the ligand backbone, allowing introduction of the amide function at either the original sp3 carbon-halide bond or at distal sp3 C-H sites within an alkyl side-chain via chain-walking scenarios.

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