16115-80-3 Usage
Description
Dimethyl aminomalonate hydrochloride, also known as aminomalonic acid dimethyl ester hydrochloride, is a hydrochloride salt of a dialkyl aminomalonate. It is a chemical compound that serves as a versatile building block in the synthesis of various organic compounds.
Uses
Used in Pharmaceutical Synthesis:
Dimethyl aminomalonate hydrochloride is used as a starting reagent in the synthesis of various pharmaceutical compounds, including methyl 3-phenyl-5-hydantoincarboxylate and Boc-Leu-Ama(OMe)2 (Boc = tert-butyloxycarbonyl, Leu = leucine, Ama = aminomalonic acid). It plays a crucial role in the development of new drugs and therapeutic agents.
Used in Chemical Synthesis:
In the chemical industry, dimethyl aminomalonate hydrochloride is used as a starting reagent for the synthesis of various organic compounds, such as (R,S)-2-phenethylcysteine hydrochloride, dimethyl 2,2,2-polynitroalkylnitroaminonitromalonates, and pirotryprostatin B. Its versatility as a synthetic building block makes it valuable in the development of new chemical products and materials.
Check Digit Verification of cas no
The CAS Registry Mumber 16115-80-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,1,1 and 5 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 16115-80:
(7*1)+(6*6)+(5*1)+(4*1)+(3*5)+(2*8)+(1*0)=83
83 % 10 = 3
So 16115-80-3 is a valid CAS Registry Number.
InChI:InChI=1/C5H9NO4.ClH/c1-9-4(7)3(6)5(8)10-2;/h3H,6H2,1-2H3;1H
16115-80-3Relevant articles and documents
Unified Strategy to Amphenicol Antibiotics: Asymmetric Synthesis of (-)-Chloramphenicol, (-)-Azidamphenicol, and (+)-Thiamphenicol and Its (+)-3-Floride
Liu, Jinxin,Li, Yaling,Ke, Miaolin,Liu, Minjie,Zhan, Pingping,Xiao, You-Cai,Chen, Fener
, p. 15360 - 15367 (2020/11/30)
The asymmetric synthesis of (-)-chloramphenicol, (-)-azidamphenicol, and (+)-thiamphenicol and its (+)-3-floride, (+)-florfenicol, is reported. This approach toward the amphenicol antibiotic family features two key steps: (1) a cinchona alkaloid derived urea-catalyzed aldol reaction allows highly enantioselective access to oxazolidinone gem-diesters and (2) a continuous flow diastereoselective decarboxylation of thermally stable oxazolidinone gem-diesters to form the desired trans-oxazolidinone monoesters with two adjacent stereocenters that provide the desired privileged scaffolds of syn-vicinal amino alcohols in the amphenicol family.
