54505-72-5 Usage
Description
DIETHYLMALONIC ACID DICHLORIDE is an organic compound that serves as an important intermediate in the synthesis of various chemical products. It is characterized by its reactivity and ability to form a wide range of derivatives, making it a versatile building block in the chemical industry.
Uses
Used in Pharmaceutical Industry:
DIETHYLMALONIC ACID DICHLORIDE is used as a synthetic intermediate for the preparation of various pharmaceutical compounds. Its ability to react with different reagents allows for the creation of a diverse range of therapeutic agents.
Used in Chemical Synthesis:
DIETHYLMALONIC ACID DICHLORIDE is used as a key building block in the synthesis of complex organic molecules. Its reactivity and compatibility with various reaction conditions make it a valuable component in the development of new chemical products.
Specific Applications:
1. Preparation of 5,5-diethyl-1,3-dihydroxybarbituric acid (N,N′-dihydroxyveronal): DIETHYLMALONIC ACID DICHLORIDE is used as a reactant in the condensation process with 1,3-dibenzyloxyurea, leading to the formation of this specific barbiturate compound.
2. Synthesis of 1,11-dibronzo-4,8-diaza-6,6-diethyl-5,7-dioxoundecaneamide containing crowned derivatives of dithiomaleonitrile: DIETHYLMALONIC ACID DICHLORIDE plays a crucial role in the synthesis of this complex molecule, showcasing its versatility in creating a wide range of chemical products.
Check Digit Verification of cas no
The CAS Registry Mumber 54505-72-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,5,0 and 5 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 54505-72:
(7*5)+(6*4)+(5*5)+(4*0)+(3*5)+(2*7)+(1*2)=115
115 % 10 = 5
So 54505-72-5 is a valid CAS Registry Number.
InChI:InChI=1/C7H10Cl2O2/c1-3-7(4-2,5(8)10)6(9)11/h3-4H2,1-2H3
54505-72-5Relevant articles and documents
Copper(II)-catalyzed enantioselective intramolecular cyclization of N-alkenylureas
Fu, Shaomin,Yang, Honghao,Deng, Yuanfu,Jiang, Huanfeng,Zeng, Wei,Li, Guoqiang
, p. 1018 - 1021 (2015/03/30)
The first Cu(II)-catalyzed highly enantioselective intramolecular cyclization of N-alkenylureas was developed for the concise assembly of chiral vicinal diamino bicyclic heterocycles. Facile removal of carbonyl group of the carbamido moiety allowed for ready access to enantioenriched cyclic vicinal diamines.
Highly enantioselective Friedel-Crafts alkylation of indoles with α,β-unsaturated ketones with simple Cu(II)-oxazoline-imidazoline catalysts
Barakat, Assem,Islam, Mohammad Shahidul,Al Majid, Abdullah M.A.,Al-Othman, Zeid Abdullah
, p. 5185 - 5192 (2013/07/05)
A series of novel chiral ligands L1-L4 with an imidazoline-oxazoline framework have been developed as new type of non-symmetric N,N-bidentate ligands. All the chiral ligands were prepared from 2,2-diethylmalonic acid and enantiomerically pure (S)-2-amino-
