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Merck
CN
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576646

Sigma-Aldrich

N -Boc-4-羟基苯胺

97%

别名:

4-(BOC-氨基)酚

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About This Item

线性分子式:
HOC6H4NHCO2C(CH3)3
CAS号:
54840-15-2
分子量:
209.24
MDL编号:
MFCD00226573
UNSPSC代码:
12352100
PubChem化学物质编号:
24880871
NACRES:
NA.22

方案

97%

mp

143-147 °C (lit.)

官能团

amine

SMILES字符串

CC(C)(C)OC(=O)Nc1ccc(O)cc1

InChI

1S/C11H15NO3/c1-11(2,3)15-10(14)12-8-4-6-9(13)7-5-8/h4-7,13H,1-3H3,(H,12,14)

InChI key

YRQMBQUMJFVZLF-UHFFFAOYSA-N

相关类别

象形图

Exclamation mark
GHS07

警示用语：

Warning

危险声明

H315,H319,H335

危险分类

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

靶器官

Respiratory system

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
0000342360
0000321942
0000321941
0000308015
0000308015

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Christopher Elam et al.
European journal of medicinal chemistry, 46(5), 1512-1523 (2011-03-01)
Two screening protocols based on recursive partitioning and computational ligand docking methodologies, respectively, were employed for virtual screens of a compound library with 345,000 entries for novel inhibitors of the enzyme sarco/endoplasmic reticulum calcium ATPase (SERCA), a potential target for
Anne Müller et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 21(39), 13723-13731 (2015-08-08)
Azobenzene linker molecules can be utilized to control peptide/protein function when they are ligated to appropriately spaced amino acid side chains of the peptide. This is because the photochemical E/Z isomerization of the azobenzene N=N double bond allows to switch

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