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4629-02-1

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4629-02-1 Usage

Type of compound

Long-chain ketone with a piperidine ring attached

Usage

Fragrance ingredient in perfumes and personal care products

Scent

Floral and musk-like

Aroma characteristics

Sweet, powdery, and slightly spicy

Potential applications

Pharmaceutical industry (medications and drug delivery systems)

Safety precautions

Handle with care and use in accordance with safety guidelines and regulations

Check Digit Verification of cas no

The CAS Registry Mumber 4629-02-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,6,2 and 9 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4629-02:
(6*4)+(5*6)+(4*2)+(3*9)+(2*0)+(1*2)=91
91 % 10 = 1
So 4629-02-1 is a valid CAS Registry Number.
InChI:InChI=1/C21H41NO/c1-2-3-4-5-6-7-8-9-10-11-12-13-15-18-21(23)22-19-16-14-17-20-22/h2-20H2,1H3

4629-02-1SDS

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 1-piperidin-1-ylhexadecan-1-one

1.2 Other means of identification

Product number -
Other names 1-(piperidin-1-yl)hexadecan-1-one

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:4629-02-1 SDS

4629-02-1Downstream Products

4629-02-1Relevant articles and documents

A Convenient Protocol for the Synthesis of Fatty Acid Amides

Johansson, Silje J. R.,Johannessen, Tonje,Ellefsen, Christiane F.,Ristun, Mali S.,Antonsen, Simen,Hansen, Trond V.,Stenstrom, Yngve,Nolsoe, Jens M. J.

supporting information, p. 213 - 217 (2019/01/14)

Several classes of biologically occurring fatty acid amides have been reported from mammalian and plant sources. Many amides conjugated with fatty acids of mammalian origin exhibit specific activation of individual receptors. Their potential as pharmacological tools or as lead compounds towards the development of novel therapeutics is of great interest. Hence, access to such amides by a practical, high-yielding and scalable protocol without affecting the geometry or position of sensitive functionalities is needed. A protocol that meets all these requirements involves activation of the corresponding acid with carbonyl diimidazole (CDI) followed by reaction with the desired amine or its hydrochloride. More than fifty compounds have been prepared in generally high yields.

A novel aromatic carbocation-based coupling reagent for esterification and amidation reactions

Nguyen, Thanh V.,Lyons, Demelza J.M.

supporting information, p. 3131 - 3134 (2015/06/17)

A novel tropylium-based coupling reagent has been developed to facilitate the synthesis of a series of esters, amides, lactones and peptides under mild reaction conditions. Remarkably, this reagent can be used in catalytic amounts in conjunction with a sacrificial reagent, offering a new and efficient method for nucleophilic coupling reactions of carboxylic acids.

Preparation and Characterization of 1,5-Diacyl-2,4-dioxohexahydro-1,3,5-triazines with Higher Acyl Groups

Hofmann, Joerg,Just, Gerhard,Pritzkow, Wilhelm

, p. 67 - 71 (2007/10/02)

The title compounds were prepared from 2,4-dioxohexahydro-triazine (DHT) and the corresponding acid chlorides in the presence of sulphuric acid.They are active acylating agents against piperidine in dioxane as the solvent.Only the diacyl derivatives of DHT with acyl chain lengths up to C6 react with aqueous solutions of sodium perborate forming the corresponding peroxy acids.

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