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57582-42-0

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  • 2,7-Naphthalenedisulfonic acid, 5-((4,6-dichloro-1,3,5-triazin-2-yl)amino)-4-hydroxy-3-((1-sulfo-2-naphthalenyl)azo)-, trisodium salt

    Cas No: 57582-42-0

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57582-42-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 57582-42-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,5,8 and 2 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 57582-42:
(7*5)+(6*7)+(5*5)+(4*8)+(3*2)+(2*4)+(1*2)=150
150 % 10 = 0
So 57582-42-0 is a valid CAS Registry Number.
InChI:InChI=1/C20H38O3/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-23-20(22)18-19(2)21/h3-18H2,1-2H3

57582-42-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name hexadecyl 3-oxobutanoate

1.2 Other means of identification

Product number -
Other names EINECS 260-825-9

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

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Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:57582-42-0 SDS

57582-42-0Downstream Products

57582-42-0Relevant articles and documents

NO-Responsive vesicles as a drug delivery system

Li, Zhi-Heng,Tan, Zheng-Li,Ding, Ai-Xiang,Gong, Bing,Lu, Zhong-Lin,He, Lan

, p. 3535 - 3538 (2017)

A rationally designed amphiphile containing a hydrophobic Hantzsch ester and a hydrophilic phosphate ester was able to form vesicles in aqueous solution, and resulted in the first example of a NO-responsive drug delivery system.

Synthesis of Fatty Acetoacetates Under Microwave Irradiation Catalysed by Sulfamic Acid in a Solvent-Free System

Weber, Andressa C. H.,Batista, Thaís C.,Gon?alves, Bruno,Hack, Carolina R. L.,Porciuncula, Larissa M.,Treptow, Tamara G. M.,D’Oca, Caroline Da R. Montes,Russowsky, Dennis,D’Oca, Marcelo G. Montes

, p. 1399 - 1406 (2016/09/28)

The 1,3-dicarbonyl compounds are important building blocks to obtain products with various biological activities and technological applications. In this work, we used a simple transesterification method to develop fatty acetoacetates in a solvent-free medium using a green catalyst, sulfamic acid (NH2SO3H), under microwave irradiation. The experimental results demonstrate good yields in a short reaction time (13?min), which makes this method an efficient approach to synthesize fatty acetoacetates from a wide range of saturated, unsaturated, and polyunsaturated long chain fatty alcohols, and ricinoleic derivatives. Experiments of recycling of the catalyst were performed and no decrease in catalytic activity of sulfamic acid was observed.

Hexamethylenetetramine-mediated transesterification of β-keto esters

Ribeiro, Rodrigo S.,De Souza, Rodrigo O. M. A.,Vasconcellos, Mario L. A. A.,Oliveira, Bianca L.,Ferreira, Leonardo C.,Aguiar, Lucia C. S.

, p. 61 - 64 (2007/12/31)

Treatment of methyl or ethyl β-keto esters with primary, secondary, or tertiary alcohols in the presence of a catalytic amount of hexamethylenetetramine results in good to high yields of the corresponding esters. Georg Thieme Verlag Stuttgart.

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