6414-58-0 Usage
General Description
DIETHYL 2-ANILINOMALONATE is a chemical compound with the molecular formula C17H19NO4. It is a colorless to light yellow liquid with a sweet, fruity odor. DIETHYL 2-ANILINOMALONATE is commonly used as an intermediate in the synthesis of pharmaceuticals, dyes, and other organic compounds. It is also used as a building block in the production of various fine chemicals and active pharmaceutical ingredients. DIETHYL 2-ANILINOMALONATE is known for its ability to undergo various chemical reactions, making it a versatile and important compound in the field of organic synthesis. It is important to handle this compound with caution and adhere to proper safety guidelines, as it may be harmful if swallowed, inhaled, or in contact with skin.
Check Digit Verification of cas no
The CAS Registry Mumber 6414-58-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,4,1 and 4 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6414-58:
(6*6)+(5*4)+(4*1)+(3*4)+(2*5)+(1*8)=90
90 % 10 = 0
So 6414-58-0 is a valid CAS Registry Number.
InChI:InChI=1/C13H17NO4/c1-3-17-12(15)11(13(16)18-4-2)14-10-8-6-5-7-9-10/h5-9,11,14H,3-4H2,1-2H3
6414-58-0Relevant articles and documents
Continuous-flow electro-oxidative coupling of sulfides with activated methylene compounds leading to sulfur ylides
Cai, Chen,Fang, Zheng,Guo, Kai,Lin, Yang,Liu, Chengkou,Yuan, Chengcheng
, p. 2956 - 2961 (2021/05/05)
An unprecedentedly straightforward electro-oxidative coupling of sulfides with activated methylene compounds to synthesize sulfur ylides has been developed. Good to excellent yields can be obtained under catalyst- and oxidant-free conditions at room tempe
A convenient synthesis of 3-phenylthio-azetidin-2-ones
Bari,Sharma,Sethi
, p. 1114 - 1119 (2007/10/03)
3-Phenylthio-4,4-diethoxycarbonyl-azetidin-2-ones 8 have been conveniently synthesised by reacting 2-chlorophenylthioacetyl chloride 5 with aryl substituted aminomalonates 7 under mild basic conditions. Alternatively, C-3 alkylation of azetidin-2-one usin