129319-91-1 Usage
Description
(R)-(-)-N-(tert-Butoxycarbonyl)-2-methylaziridine is a chemical compound belonging to the aziridine class. It is also referred to as Boc-protected aziridine due to the presence of the tert-Butoxycarbonyl (Boc) protecting group. (R)-(-)-N-(tert-Butoxycarbonyl)-2-methylaziridine features a chiral center with the (R)-(-) configuration, making it a valuable building block in organic synthesis for creating a variety of nitrogen-containing compounds. The Boc group is crucial for controlling the reactivity and selectivity of the aziridine ring during chemical reactions, while the 2-methylaziridine moiety introduces steric hindrance, affecting the compound's reactivity and stability.
Uses
Used in Pharmaceutical Industry:
(R)-(-)-N-(tert-Butoxycarbonyl)-2-methylaziridine is used as an intermediate in the synthesis of various pharmaceutical compounds for [application reason, e.g., targeting specific biological pathways or enhancing drug efficacy].
Used in Chemical Research:
In the field of chemical research, (R)-(-)-N-(tert-Butoxycarbonyl)-2-methylaziridine is used as a versatile building block for [application reason, e.g., exploring new reaction mechanisms or developing novel synthetic methods].
Used in Material Science:
(R)-(-)-N-(tert-Butoxycarbonyl)-2-methylaziridine is employed as a key component in the development of advanced materials for [application reason, e.g., creating new polymers with specific properties or improving existing material systems].
Check Digit Verification of cas no
The CAS Registry Mumber 129319-91-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,3,1 and 9 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 129319-91:
(8*1)+(7*2)+(6*9)+(5*3)+(4*1)+(3*9)+(2*9)+(1*1)=141
141 % 10 = 1
So 129319-91-1 is a valid CAS Registry Number.
129319-91-1Relevant articles and documents
Protected Chloroethyl and Chloropropyl Amines as Conformationally Unrestricted Annulating Reagents
Shi, Qing,Meehan, Mariah C.,Galella, Michael,Park, Hyunsoo,Khandelwal, Purnima,Hynes, John,Dhar, T. G. Murali,Marcoux, David
supporting information, p. 337 - 340 (2018/01/28)
The purpose of this letter is to document the use of protected chloroethyl and chloropropyl amines as conformationally unrestricted ambiphilic reagents that undergo annulation reactions with Michael acceptors. This reaction is wide in scope and utilizes r
NOVEL COMPOUNDS AS CANNABINOID RECEPTOR LIGANDS
-
Page/Page column 40, (2009/10/06)
Disclosed herein are compounds of formula (I) wherein R1, R2, R3, R25a, R26a, X, and n are as defined in the specification. Pharmaceutical compositions comprising such compounds, and methods of treating conditions and disorders using such compounds and pharmaceutical compositions are also described
Asymmetric synthesis of α-alkylated aldehydes using terminal epoxide-derived chiral enamines
Hodgson, David M.,Kaka, Naeem S.
supporting information; experimental part, p. 9958 - 9960 (2009/06/30)
(Chemical Equation Presented) Effective discrimination: Efficient lithium amide-induced terminal epoxide-enamine transformation provides the first enamines capable of generating α-alkylated aldehydes with high asymmetric induction by intermolecular nucleophilic substitution (see scheme).
