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Merck
CN

07858

Sigma-Aldrich

(R)-3-氨基-1-叔丁氧羰基哌啶

≥98.0% (TLC)

别名:

(R)-1-Boc-3-氨基哌啶, (R)-1-叔丁氧羰基-3-氨基哌啶

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About This Item

经验公式(希尔记法):
C10H20N2O2
分子量:
200.28
MDL编号:
UNSPSC代码:
12352005
PubChem化学物质编号:
NACRES:
NA.22

质量水平

检测方案

≥98.0% (TLC)

旋光性

[α]/D -28.5±2°, c = 1 in DMF

SMILES字符串

CC(C)(C)OC(=O)N1CCC[C@@H](N)C1

InChI

1S/C10H20N2O2/c1-10(2,3)14-9(13)12-6-4-5-8(11)7-12/h8H,4-7,11H2,1-3H3/t8-/m1/s1

InChI key

AKQXKEBCONUWCL-MRVPVSSYSA-N

一般描述

(R)-3-Amino-1-Boc-piperidine can be used as a precursor for the preparation of dipeptidyl peptidase IV inhibitors like linagliptin, alogliptin, and other antidiabetic agents.

应用

(R)-3-Amino-1-Boc-piperidine can be used to prepare a benzoxazepine derivative named (R)-7-(3,5-dimethoxyphenyl)-N-(piperidin-3-yl)-4-propionyl-2,3,4,5-tetrahydro-1,4-benzoxazepine-9-carboxamide, a potent CBP/P300 bromodomain inhibitor.

象形图

Exclamation mark

警示用语:

Warning

危险分类

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

靶器官

Respiratory system

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

法规信息

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分析证书(COA)

Lot/Batch Number

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访问文档库

Development of selective CBP/P300 benzoxazepine bromodomain inhibitors
Popp TA, et al.
Journal of Medicinal Chemistry, 59(19), 8889-8912 (2016)
Asymmetric synthesis of a high added value chiral amine using immobilized ω-transaminases
Petri A, et al.
Beilstein Journal of Organic Chemistry, 15(1), 60-66 (2019)

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