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

23054-48-0

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23054-48-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 23054-48-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,0,5 and 4 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 23054-48:
(7*2)+(6*3)+(5*0)+(4*5)+(3*4)+(2*4)+(1*8)=80
80 % 10 = 0
So 23054-48-0 is a valid CAS Registry Number.

23054-48-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(2-hydroxyethyl)cyclohexanecarboxamide

1.2 Other means of identification

Product number -
Other names cyclohexanecarboxylic acid 2-hydroxy-ethylamide

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:23054-48-0 SDS

23054-48-0Relevant academic research and scientific papers

Tandem Photoredox Catalysis: Enabling Carbonylative Amidation of Aryl and Alkylhalides

Connell, Timothy U.,Forni, José A.,Micic, Nenad,Polyzos, Anastasios,Weragoda, Geethika

supporting information, p. 18646 - 18654 (2020/08/21)

We report a new visible-light-mediated carbonylative amidation of aryl, heteroaryl, and alkyl halides. A tandem catalytic cycle of [Ir(ppy)2(dtb-bpy)]+ generates a potent iridium photoreductant through a second catalytic cycle in the presence of DIPEA, which productively engages aryl bromides, iodides, and even chlorides as well as primary, secondary, and tertiary alkyl iodides. The versatile in situ generated catalyst is compatible with aliphatic and aromatic amines, shows high functional-group tolerance, and enables the late-stage amidation of complex natural products.

Synthesis of Aliphatic Amides through a Photoredox Catalyzed Radical Carbonylation Involving Organosilicates as Alkyl Radical Precursors

Cartier, Alex,Levernier, Etienne,Dhimane, Anne-Lise,Fukuyama, Takahide,Ollivier, Cyril,Ryu, Ilhyong,Fensterbank, Louis

, p. 2254 - 2259 (2020/05/06)

Alkyl radicals, from primary to tertiary, formed by photocatalyzed oxidation of organosilicates, are involved efficiently in radical carbonylation with carbon monoxide (CO), in the presence of various amines and CCl4, leading to a variety of amides in moderate to good yields. (Figure presented.).

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