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Diethyl butyl(phenyl)propanedioate is a complex organic compound with the chemical formula C21H30O4. It is an ester derivative of diethyl propanedioate (also known as diethyl malonate), where one of the hydrogen atoms on the propanedioate moiety is replaced by a butyl group and a phenyl group. diethyl butyl(phenyl)propanedioate is characterized by its long, branched hydrocarbon chain and aromatic ring, which contribute to its unique chemical properties. It is typically synthesized through a series of chemical reactions and is used in various industrial applications, such as the production of fragrances, pharmaceuticals, and other specialty chemicals. Due to its specific structure, diethyl butyl(phenyl)propanedioate exhibits unique solubility and reactivity profiles, making it a valuable component in the synthesis of more complex molecules.

7155-21-7

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7155-21-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7155-21-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,5 and 5 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 7155-21:
(6*7)+(5*1)+(4*5)+(3*5)+(2*2)+(1*1)=87
87 % 10 = 7
So 7155-21-7 is a valid CAS Registry Number.

7155-21-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name diethyl 2-butyl-2-phenylpropanedioate

1.2 Other means of identification

Product number -
Other names Butyl-phenyl-malonsaeure-diaethylester

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:7155-21-7 SDS

7155-21-7Relevant academic research and scientific papers

Chemiluminiscent Thermolysis of a Peroxylactones

Turro, Nicolas J.,Chow, Ming-Fea

, p. 5058 - 5064 (2007/10/02)

A comprehensive study of the chemiluminiscent decomposition of a three α-peroxylactones (dimethyl α-peroxylactone (1), phenyl n-butyl α-peroxylactone (2), and diphenyl α-peroxylactone (3)) has been undertaken.Each compound decomposes to yield CO2 and the corresponding ketone in a high yield.The chemiluminiscent species produced in these reactions have been characterized by a number of different measurements including distribution of direct chemiluminiscence, lifetimes, energy transfer, activation parameters, and photochemical reactions.Excited state chemiexcitation efficiences have also been evaluated.It is shown that a combination of conventional kinetic measurements and "step analysis" of the chemiluminiscence intensivity provides a means of evaluating the activation energies for the deactivation paths of electronically excited states that precede the emission step responsible for chemiluminiscence.The latter activation energies may also be monitored directly in some cases by measurement of excited-state lifetimes as a function of temperature.The agreement between the activation energies generated from chemiluminiscence data and direct photoexcitation measurements is within the experimental error.The results for 1 are compared to those for tetramethyldioxetane (4) (both produce electronically excited acetone) and are found to be in excellent agreement.

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