10471-28-0 Usage
Description
DODECANEDIOIC ACID DIETHYL ESTER, also known as Ethyl 11-Ethoxycarbonyldodecanoate (CAS# 10471-28-0), is a colorless oil compound that is useful in organic synthesis. It is a diester derived from dodecanedioic acid and is known for its versatile chemical properties.
Uses
Used in Organic Synthesis:
DODECANEDIOIC ACID DIETHYL ESTER is used as a synthetic intermediate for the production of various chemicals and materials. Its ability to undergo various chemical reactions makes it a valuable component in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in the Chemical Industry:
In the chemical industry, DODECANEDIOIC ACID DIETHYL ESTER is used as a building block for the creation of complex molecules and polymers. Its compatibility with a wide range of reagents and its stability under various reaction conditions contribute to its utility in this field.
Used in the Pharmaceutical Industry:
DODECANEDIOIC ACID DIETHYL ESTER is used as a key component in the development of new drugs and drug candidates. Its unique chemical structure allows for the design of novel molecules with potential therapeutic applications.
Used in the Agrochemical Industry:
In the agrochemical industry, DODECANEDIOIC ACID DIETHYL ESTER is used as a starting material for the synthesis of various pesticides and other agricultural chemicals. Its versatility in chemical reactions enables the development of new products with improved performance and reduced environmental impact.
Used in the Polymer Industry:
DODECANEDIOIC ACID DIETHYL ESTER is used as a monomer or additive in the production of polymers and plastics. Its incorporation into polymer formulations can enhance properties such as strength, flexibility, and durability, leading to the development of new materials with specific applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 10471-28-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,4,7 and 1 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 10471-28:
(7*1)+(6*0)+(5*4)+(4*7)+(3*1)+(2*2)+(1*8)=70
70 % 10 = 0
So 10471-28-0 is a valid CAS Registry Number.
InChI:InChI=1/C16H30O4/c1-3-19-15(17)13-11-9-7-5-6-8-10-12-14-16(18)20-4-2/h3-14H2,1-2H3
10471-28-0Relevant articles and documents
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Cumper,C.W.N. et al.
, p. 2067 - 2072 (1965)
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Ni/Co-catalyzed homo-coupling of alkyl tosylates
Komeyama, Kimihiro,Tsunemitsu, Ryusuke,Michiyuki, Takuya,Yoshida, Hiroto,Osaka, Itaru
, (2019/05/02)
A direct reductive homo-coupling of alkyl tosylates has been developed by employing a combination of nickel and nucleophilic cobalt catalysts. A single-electron-transfer-type oxidative addition is a pivotal process in the well-established nickel-catalyzed coupling of alkyl halides. However, the method cannot be applied to the homo-coupling of ubiquitous alkyl tosylates due to the high-lying σ*(C–O) orbital of the tosylates. This paper describes a Ni/Co-catalyzed protocol for the activation of alkyl tosylates on the construction of alkyl dimers under mild conditions.
One-pot synthesis of cyclophane-type macrocycles using manganese(iii)- mediated oxidative radical cyclization
Ito, Yosuke,Tomiyasu, Yuichi,Kawanabe, Takahiro,Uemura, Keisuke,Ushimizu, Yuu,Nishino, Hiroshi
supporting information; scheme or table, p. 1491 - 1507 (2011/04/23)
Cyclophane-type macrocyclic compounds from 21 to 56 members having two fused dihydrofuran rings were synthesized by the manganese(iii)-mediated oxidation of terminal dienes with bis(3-oxobutanoate)s containing aromatics. The reaction detail, characterization and reaction pathways are described. The Royal Society of Chemistry 2011.
