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16424-30-9

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16424-30-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16424-30-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,4,2 and 4 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 16424-30:
(7*1)+(6*6)+(5*4)+(4*2)+(3*4)+(2*3)+(1*0)=89
89 % 10 = 9
So 16424-30-9 is a valid CAS Registry Number.

16424-30-9SDS

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 5-Oxomyristinsaeure-methylester

1.2 Other means of identification

Product number -
Other names 5-Oxo-tetradecansaeure-methylester

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:16424-30-9 SDS

16424-30-9Downstream Products

16424-30-9Relevant articles and documents

Regioselective Functionalization of Nonactivated CH-Bonds, 4. -Photoreactions of Amphiphilic Derivatives of Benzophenonecarboxylic Acid and Myristic Acid Derivatives in Micelles and Bilayers

Gogoll, Adolf,Schaefer, Hans J.

, p. 597 - 606 (2007/10/02)

Amphiphilic derivatives of benzophenonecarboxylic acid and myristic acid in micelles, vesicles, and multilamellar aggregates were photochemically converted into tertiary alcohols, the workup of which yielded mixtures of the isomeric ketomyristic acid methyl esters 5.A slightly increased but none the less low selectivity was found in bilayers in comparison with micelles.Various amphiphilic head groups shifted the center of attack.Low total yields, especially in bilayers, can be attributed to a predominant reaction between the benzophenone substituents.By preparation of the corresponding reference compounds it could be demonstrated that benzhydrols (8a-d) or benzpinacols (9a-c) are not formed in this unexpected reaction.

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