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576646

Sigma-Aldrich

N-Boc-4-hydroxyaniline

97%

Synonym(s):

N-Boc-4-aminophenol

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About This Item

Linear Formula:
HOC6H4NHCO2C(CH3)3
CAS Number:
54840-15-2
Molecular Weight:
209.24
MDL number:
MFCD00226573
UNSPSC Code:
12352100
PubChem Substance ID:
24880871
NACRES:
NA.22

assay

97%

mp

143-147 °C (lit.)

functional group

amine

SMILES string

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

Related Categories

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
0000308015
0000321942
0000321941
0000342360
BGBC1630V

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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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