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TRIETHYL 3-ACETYLPENTANE-1,3,5-TRICARBOXYLATE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

72948-75-5

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72948-75-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 72948-75-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,9,4 and 8 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 72948-75:
(7*7)+(6*2)+(5*9)+(4*4)+(3*8)+(2*7)+(1*5)=165
165 % 10 = 5
So 72948-75-5 is a valid CAS Registry Number.

72948-75-5SDS

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 triethyl 3-acetylpentane-1,3,5-tricarboxylate

1.2 Other means of identification

Product number -
Other names Triethyl 3-acetyl-1,3,5-pentanetricarboxylate

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:72948-75-5 SDS

72948-75-5Relevant academic research and scientific papers

A Molecular Torsion Balance Study: A Nearby Anionic Group Exerts Little Influence on Hydrophobic Interactions between Nonpolar Surfaces

Ling, Xiujun,Wilcox, Craig S.

supporting information, p. 14010 - 14014 (2019/11/14)

Polar groups have a solvent ordering effect on water and therefore may affect hydrophobic binding energies for nearby lipophilic surfaces. This would mean that determinations of excess surface free energy association energies require consideration of nearby polar functional groups. This paper reports results of a study to measure this possible effect. It was concluded from the models used here that an anionic polar group nearby a hydrophobic surface has little or no effect on the magnitude of hydrophobic association.

A simple, efficient and green procedure for Michael addition catalyzed by [C4dabco]OH ionic liquid

Keithellakpam, Sanjoy,Laitonjam, Warjeet S.

, p. 767 - 770 (2014/06/09)

A dabco-based basic ionic liquid, 1-butyl-4-aza-1-azaniabicyclo[2.2.2] octane hydroxide, has been developed as a catalyst for a convenient and rapid method for the Michael addition of active methylene compounds to α,β-unsaturated carboxylic esters and nitriles. The method is very simple, and the yields are very high. The catalyst can be recycled several times without much loss of activity.

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