71811-26-2 Usage
Description
N-Cbz-2-Amino-1,3-propanediol, also known as Z-2-amino-1,3-propanediol, is a white to off-white crystalline chemical compound with a molecular formula of C10H17NO2 and a molecular weight of 183.25 g/mol. It is widely recognized for its role as a reagent in organic synthesis and as a chiral building block in the production of pharmaceuticals and agrochemicals. N-Cbz-2-Amino-1,3-propanediol is also utilized as a key intermediate in the synthesis of various hetero-aromatic compounds and in the preparation of chiral amines, making it an essential component in the field of organic synthesis.
Uses
Used in Pharmaceutical Industry:
N-Cbz-2-Amino-1,3-propanediol is used as a chiral building block for the production of pharmaceuticals, contributing to the development of new drugs with improved efficacy and selectivity. Its chiral nature allows for the creation of enantiomerically pure compounds, which is crucial for the synthesis of biologically active molecules.
Used in Agrochemical Industry:
In the agrochemical industry, N-Cbz-2-Amino-1,3-propanediol serves as a chiral building block for the synthesis of agrochemicals, such as pesticides and herbicides. Its use in this industry helps in the development of more effective and environmentally friendly products.
Used in Organic Synthesis:
N-Cbz-2-Amino-1,3-propanediol is used as a key intermediate in the synthesis of various hetero-aromatic compounds, which are important in the development of new organic compounds with potential applications in various fields.
Used in Chiral Amine Preparation:
N-Cbz-2-Amino-1,3-propanediol is utilized in the preparation of chiral amines, which are essential building blocks in the synthesis of a wide range of biologically active molecules, including pharmaceuticals and agrochemicals.
Used in Asymmetric Synthesis:
N-Cbz-2-Amino-1,3-propanediol is employed as a chiral reagent in asymmetric synthesis, enabling the creation of other chiral molecules with high enantioselectivity. This is crucial for the development of enantiomerically pure compounds with specific biological activities.
Check Digit Verification of cas no
The CAS Registry Mumber 71811-26-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,8,1 and 1 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 71811-26:
(7*7)+(6*1)+(5*8)+(4*1)+(3*1)+(2*2)+(1*6)=112
112 % 10 = 2
So 71811-26-2 is a valid CAS Registry Number.
InChI:InChI=1/C11H15NO4/c13-6-10(7-14)12-11(15)16-8-9-4-2-1-3-5-9/h1-5,10,13-14H,6-8H2,(H,12,15)
71811-26-2Relevant articles and documents
An M2-V27A channel blocker demonstrates potent in?vitro and in?vivo antiviral activities against amantadine-sensitive and -resistant influenza A viruses
Hu, Yanmei,Musharrafieh, Rami,Ma, Chunlong,Zhang, Jiantao,Smee, Donald F.,DeGrado, William F.,Wang, Jun
, p. 45 - 54 (2017/01/25)
Adamantanes such as amantadine (1) and rimantadine (2) are FDA-approved anti-influenza drugs that act by inhibiting the wild-type M2 proton channel from influenza A viruses, thereby inhibiting the uncoating of the virus. Although adamantanes have been suc
Novel 2,5-Disubstituted 1,3-dioxanes and oxazolidines as potential chemoprevention agents and building blocks for organic synthesis
Rueger, Anne J.,Nieger, Martin,Es-Sayed, Maezen,Braese, Stefan
experimental part, p. 3837 - 3846 (2010/09/10)
2,5-Disubstituted 1,3-dioxacycloalkanes have recently been found to be promising lead, compounds that possess potent anti-inflammatory activity and therefore may act as chemoprevention agents. Encouraged by this we have designed and synthesized a new seri
Highly efficient synthesis of enantiomerically enriched 2-hydroxymethylaziridines by enzymatic desymmetrization
Jun, Young Choi,Borch, Richard F.
, p. 215 - 218 (2007/10/03)
(Chemical Equation Presented) Both enantiomers of protected and unprotected 2-hydroxymethylaziridines are efficiently and enantiospecifically synthesized by using a combination of enzymatic and synthetic methods. PPL was used for lipase-catalyzed desymmet