tert-Butyl (1-(2-nitrophenyl)piperidin-4-yl)carbamate

Base Information

• Chemical Name: tert-Butyl (1-(2-nitrophenyl)piperidin-4-yl)carbamate
• CAS No.: 1023594-62-8
• Molecular Formula: C16H23N3O4
• Molecular Weight: 321.37152
• Hs Code.: 2933399090
• DSSTox Substance ID: DTXSID10693169
• Wikidata: Q82622191
• Mol file: 1023594-62-8.mol

Synonyms:1023594-62-8;tert-Butyl (1-(2-nitrophenyl)piperidin-4-yl)carbamate;tert-butyl N-[1-(2-nitrophenyl)piperidin-4-yl]carbamate;tert-Butyl 1-(2-nitrophenyl)piperidin-4-ylcarbamate;tert-Butyl [1-(2-nitrophenyl)piperidin-4-yl]carbamate;SCHEMBL3955951;tert-Butyl(1-(2-nitrophenyl)piperidin-4-yl)carbamate;DTXSID10693169;TWVQFWFIVYGRGW-UHFFFAOYSA-N;AKOS008748260;KS-5473;FT-0713192;tert-butyl 1-(2-nitro phenyl)piperidin-4-ylcarbamate;F1911-3640;[1-(2-Nitro-phenyl)-piperidin-4-yl]-carbamic acid tert-butyl ester

Chemical Property of tert-Butyl (1-(2-nitrophenyl)piperidin-4-yl)carbamate

Chemical Property:

• PSA: 90.88000
• LogP: 3.88090
• Storage Temp.: 2-8°C
• XLogP3: 3.1
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 4
• Exact Mass: 321.16885622
• Heavy Atom Count: 23
• Complexity: 422

Purity/Quality:

98%min ^*data from raw suppliers

tert-Butyl(1-(2-nitrophenyl)piperidin-4-yl)carbamate 95+% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC(C)(C)OC(=O)NC1CCN(CC1)C2=CC=CC=C2[N+](=O)[O-]
• Uses: tert-Butyl (1-(2-nitrophenyl)piperidin-4-yl)carbamate is used as a reactant in the preparation of heteroaryl amides as PIM kinase inhibitors for treating cancer.

Technology Process of tert-Butyl (1-(2-nitrophenyl)piperidin-4-yl)carbamate

There total 1 articles about tert-Butyl (1-(2-nitrophenyl)piperidin-4-yl)carbamate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 100.0%

→ tert-butyl 1-(2-nitrophenyl)piperidin-4-ylcarbamate (1023594-62-8)

Guidance literature:

Refernces

• 1、 -. "ANILINOPIPERAZINE DERIVATIVES AND METHODS OF USE THEREOF". Page/Page column 185. . Retrieved 2008/12/05.