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6786-36-3

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6786-36-3 Usage

General Description

N-Octadecanophenone is a chemical compound with the molecular formula C18H27NO. It is a ketone that is used as a fragrance ingredient and as a flavoring agent in the food industry. N-octadecanophenone is also utilized in the manufacturing of various products such as soaps, cosmetics, and perfumes. Additionally, it has been studied for its potential antimicrobial and anti-inflammatory properties and has found applications in pharmaceutical research. N-OCTADECANOPHENONE is not considered to be highly hazardous, but as with any chemical, proper handling and storage procedures should be followed to ensure safety.

Check Digit Verification of cas no

The CAS Registry Mumber 6786-36-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,7,8 and 6 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6786-36:
(6*6)+(5*7)+(4*8)+(3*6)+(2*3)+(1*6)=133
133 % 10 = 3
So 6786-36-3 is a valid CAS Registry Number.
InChI:InChI=1/C24H40O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-19-22-24(25)23-20-17-16-18-21-23/h16-18,20-21H,2-15,19,22H2,1H3

6786-36-3 Well-known Company Product Price

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  • Alfa Aesar

  • (H53394)  n-Octadecanophenone, 99%   

  • 6786-36-3

  • 1g

  • 274.0CNY

  • Detail
  • Alfa Aesar

  • (H53394)  n-Octadecanophenone, 99%   

  • 6786-36-3

  • 5g

  • 1029.0CNY

  • Detail
  • Alfa Aesar

  • (H53394)  n-Octadecanophenone, 99%   

  • 6786-36-3

  • 25g

  • 4116.0CNY

  • Detail

6786-36-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Octadecanophenone

1.2 Other means of identification

Product number -
Other names 1-Octadecanone, 1-phenyl-

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:6786-36-3 SDS

6786-36-3Relevant articles and documents

Palladium catalyzed decarboxylative acylation of arylboronic acid with ethyl cyanoacetate as a new acylating agent: Synthesis of alkyl aryl ketones

Yousuf, Md,Das, Tuluma,Adhikari, Susanta

, p. 8763 - 8770 (2015/11/10)

Palladium catalyzed acylation of arylboronic acid containing various functional groups was performed efficiently by ethyl cyanoacetate/substituted ethyl cyanoacetate as the acylating agent in aqueous triflic acid medium. The alkyl aryl ketones were obtained in good to excellent yields, first by addition of arylboronic acid to the nitrile group of ethyl cyanoacetate and their derivatives, followed by in situ decarboxylation of the resulting β-ketoester.

Acylative Suzuki coupling of amides: Acyl-nitrogen activation via synergy of independently modifiable activating groups

Li, Xijing,Zou, Gang

supporting information, p. 5089 - 5092 (2015/03/30)

A highly efficient palladium-catalyzed acylative cross-coupling of carboxylic amides with arylboronic acids has been achieved via synergistic activation of the Cacyl-N bond by independently modifiable activating groups. Coupling of amides features not only good functional group tolerance but also modifiable reactivities to overcome steric hindrance. This journal is

Liquid-crystalline polymorphism of symmetrical azobananas: Bis(4-(4-alkylphenyl)azophenyl) 2-nitroisophtalates

Zygadlo,Dardas,Nowicka,Hofmann,Galewski

scheme or table, p. 283 - 291 (2011/08/02)

In this paper we present a series of novel compounds, bis(4-(4-alkylphenyl) azophenyl) 2-nitroisophtalates, which exhibit nematic and banana-type liquidcrystalline phases. The alkyl chain length varies from 1 to 18 carbons. The first ten members of this series exhibit nematic phase. The last eleven compounds exhibit banana-type liquid crystalline phases. The propyl and pentyl derivatives have extra second type of banana mesophase. Copyright Taylor & Francis Group, LLC.

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