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56630-42-3

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56630-42-3 Usage

Type of compound

Unsaturated fatty acid derivative

Structure

Contains a long hydrocarbon chain attached to a piperidine ring

Applications

Used in the synthesis of various pharmaceuticals and bioactive molecules

Potential properties

Studied for its potential antifungal and antimicrobial properties

Safety precautions

Important to handle with care due to potential health hazards

Usage setting

Should be used in a controlled laboratory setting

Field of application

Versatile compound with potential applications in medicinal chemistry and drug development

Check Digit Verification of cas no

The CAS Registry Mumber 56630-42-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,6,3 and 0 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 56630-42:
(7*5)+(6*6)+(5*6)+(4*3)+(3*0)+(2*4)+(1*2)=123
123 % 10 = 3
So 56630-42-3 is a valid CAS Registry Number.

56630-42-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-piperidin-1-yloctadec-9-en-1-one

1.2 Other means of identification

Product number -
Other names 1-octadec-9-enoyl-piperidine

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:56630-42-3 SDS

56630-42-3Relevant articles and documents

Direct Aminolysis of Nonactivated and Thermally Unstable Esters at High Pressure

Matsumoto, Kiyoshi,Hashimoto, Shiro,Uchida, Takane,Okamoto, Tadashi,Otani, Shinichi

, p. 1357 - 1364 (2007/10/02)

The preparation of the amides 3 from a wide variety of nonactivated esters 1 and secondary amines 2 has been achieved at 8 kbar and around 45 deg C; scope and limitations are discussed.The method was also successfully applied for the aminolysis of alkyl 2-arylsulfinylacetates 7 that are relatively sensitive to heat. - Key Words: Aminolysis/ High-pressure synthesis

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