211310-10-0 Usage
Description
1-BOC-2-(METHOXY-METHYL-CARBAMOYL)PIPERIDINE is a white solid chemical compound belonging to the class of piperidine derivatives. It has a molecular formula of C13H24N2O3 and a molecular weight of 256.34 g/mol. 1-BOC-2-(METHOXY-METHYL-CARBAMOYL)PIPERIDINE is an important intermediate in the synthesis of various pharmaceutical drugs, agrochemicals, and other fine chemicals due to its BOC group.
Uses
Used in Pharmaceutical Research and Organic Synthesis:
1-BOC-2-(METHOXY-METHYL-CARBAMOYL)PIPERIDINE is used as a reagent in organic synthesis and pharmaceutical research for its ability to act as a useful intermediate in the synthesis of various pharmaceutical drugs, agrochemicals, and other fine chemicals.
Used as a Protecting Group in Organic Chemistry:
In the field of organic chemistry, 1-BOC-2-(METHOXY-METHYL-CARBAMOYL)PIPERIDINE is used as a protecting group for amines and other reactive functional groups, which is crucial for the synthesis of complex organic molecules.
Used in the Preparation of Peptide and Peptide-Based Compounds:
1-BOC-2-(METHOXY-METHYL-CARBAMOYL)PIPERIDINE also finds applications in the preparation of peptide and peptide-based compounds, which are essential in the development of new drugs and therapeutic agents.
Overall, 1-BOC-2-(methoxy-methyl-carbamoyl)piperidine is an important chemical intermediate with diverse applications in the field of drug discovery and organic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 211310-10-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,1,3,1 and 0 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 211310-10:
(8*2)+(7*1)+(6*1)+(5*3)+(4*1)+(3*0)+(2*1)+(1*0)=50
50 % 10 = 0
So 211310-10-0 is a valid CAS Registry Number.
211310-10-0Relevant articles and documents
Construction of azaspirocyclic skeletons mediated by the carbonyl of the Weinreb amide: Formal total synthesis of (±)-cephalotaxine
Ding, Huili,Fan, Yuxue,Jiang, Minghua,Li, Shanshan,Liu, Jianyin,Liu, Lu,Liu, Tianfu,Zhang, Jian
supporting information, p. 1879 - 1882 (2022/03/15)
A facile Stevens rearrangement of the Weinreb amide and the subsequent key steps mediated by the carbonyl of the Weinreb amide led to the construction of azaspirocyclic skeletons of some typical alkaloids. And the formal total synthesis of (±)-cephalotaxine was completed via a shorter synthetic route by this efficient method. Further studies on the development and asymmetric synthesis application of this strategy are underway. This journal is
MODIFIED PROTEINS AND PROTEIN DEGRADERS
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Paragraph 001422-001424, (2021/12/08)
Provided herein are compounds, pharmaceutical compositions, and methods for binding or degrading target proteins. Further provided herein are compounds having a DNA damage-binding protein 1 (DDB1) binding moiety. Some such embodiments include a linker. Some such embodiments include a target protein binding moiety. Further provided herein are ligand-DDB1 complexes. Further provided herein are in vivo modified DDB1 proteins.
Rh2(II)-catalyzed selective aminomethylene migration from styryl azides
Kong, Chen,Jana, Navendu,Driver, Tom G.
, p. 824 - 827 (2013/03/29)
Rh2(II)-Carboxylate complexes were discovered to promote the selective migration of aminomethylenes in β,β-disubstituted styryl azides to form 2,3-disubstituted indoles. Mechanistic data are also presented that suggest that the migration occurs stepwise before diffusion of the iminium ion.