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1674-38-0

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1674-38-0 Usage

Description

LAUROPHENONE, also known as 1-Phenyldodecan-1-one, is a white to beige crystalline mass or powder with unique chemical properties. It is a compound that has garnered interest due to its potential applications in various fields.

Uses

Used in Analytical Chemistry:
LAUROPHENONE is used as a component in micellar electrokinetic chromatography (MEC) systems for its ability to enhance the separation and analysis of various compounds. Its inclusion in MEC systems improves the efficiency and accuracy of the chromatographic process, making it a valuable tool in analytical chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 1674-38-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,7 and 4 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1674-38:
(6*1)+(5*6)+(4*7)+(3*4)+(2*3)+(1*8)=90
90 % 10 = 0
So 1674-38-0 is a valid CAS Registry Number.
InChI:InChI=1/C17H26O/c1-2-3-4-5-6-7-8-12-15-17(18)16-13-10-9-11-14-16/h9-11,13-14H,2-8,12,15H2,1H3

1674-38-0 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
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  • Detail
  • Alfa Aesar

  • (L02014)  Dodecanophenone, 97%   

  • 1674-38-0

  • 25g

  • 406.0CNY

  • Detail
  • Alfa Aesar

  • (L02014)  Dodecanophenone, 97%   

  • 1674-38-0

  • 100g

  • 1452.0CNY

  • Detail

1674-38-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name Dodecanophenone

1.2 Other means of identification

Product number -
Other names Phenyl Undecyl Ketone

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:1674-38-0 SDS

1674-38-0Relevant articles and documents

Nickel-Mediated Photoreductive Cross Coupling of Carboxylic Acid Derivatives for Ketone Synthesis**

Brauer, Jan,Quraishi, Elisabeth,Kammer, Lisa Marie,Opatz, Till

supporting information, p. 18168 - 18174 (2021/11/30)

A simple visible light photochemical, nickel-catalyzed synthesis of ketones from carboxylic acid-derived precursors is presented. Hantzsch ester (HE) functions as a cheap, green and strong photoreductant to facilitate radical generation and also engages in the Ni-catalytic cycle to restore the reactive species. With this dual role, HE allows for the coupling of a large variety of radicals (1°,2°, benzylic, α-oxy & α-amino) with aroyl and alkanoyl moieties, a new feature in reactions of this type. With both precursors deriving from abundant carboxylic acids, this protocol is a welcome addition to the organic chemistry toolbox. The reaction proceeds under mild conditions without the need for toxic metal reagents or bases and shows a wide scope, including pharmaceuticals and complex molecular architectures.

PROCESS FOR THE PREPARATION OF ALKOXYLATES COMPOSITIONS

-

Page/Page column 23, (2019/06/17)

A mixture of two alkoxylates surfactants, one being an aryl aliphatic carbinol alkoxylate, the other one being a dialiphatic carbinol alkoxylate, said mixture being useful for stabilizing emulsions and dispersions used in agricultural or pharmaceutical formulations. The alkoxylates surfactants may serve as substitutes for nonylphenol ethoxylates (NPE) and tristyrylphenol ethoxylates (TSE).

Nickel-Catalyzed Alkylation of Ketone Enolates: Synthesis of Monoselective Linear Ketones

Das, Jagadish,Vellakkaran, Mari,Banerjee, Debasis

, p. 769 - 779 (2019/01/24)

Herein we have developed a Ni-catalyzed protocol for the synthesis of linear ketones. Aryl, alkyl, and heteroaryl ketones as well as alcohols yielded the monoselective ketones in up to 90% yield. The catalytic protocol was successfully applied in to a gram-scale synthesis. For a practical utility, applications of a steroid derivative, oleyl alcohol, and naproxen alcohol were employed. Preliminary catalytic investigations involving the isolation of a Ni intermediate and defined Ni-H species as well as a series of deuterium-labeling experiments were performed.

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