Skip to Content
Merck
All Photos(2)

Key Documents

View All Documentation

576646

Sigma-Aldrich

N-Boc-4-hydroxyaniline

97%

Synonym(s):

N-Boc-4-aminophenol

Sign Into View Organizational & Contract Pricing
All Photos(2)

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

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
0000308015
0000321942
0000321941
0000342360
BGBC1630V

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

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

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service