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Sigma-Aldrich

4-[(N-Boc)aminomethyl]aniline

97%

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About This Item

Linear Formula:
H2NC6H4CH2NHCO2C(CH3)3
CAS Number:
94838-55-8
Molecular Weight:
222.28
MDL number:
MFCD03001716
UNSPSC Code:
12352100
PubChem Substance ID:
24874499
NACRES:
NA.22

Quality Level

100

Assay

97%

mp

75-78 °C (lit.)

functional group

amine

SMILES string

CC(C)(C)OC(=O)NCc1ccc(N)cc1

InChI

1S/C12H18N2O2/c1-12(2,3)16-11(15)14-8-9-4-6-10(13)7-5-9/h4-7H,8,13H2,1-3H3,(H,14,15)

InChI key

UXWQXBSQQHAGMG-UHFFFAOYSA-N

General description

4-[(N-Boc)aminomethyl]aniline is a protected amine.

Application

4-[(N-Boc)aminomethyl]aniline may be used in the synthesis of haptens and 4-(N-boc-aminomethyl)benzene diazonium tetrafluoroborate salt.

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

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Certificates of Analysis (COA)

Lot/Batch Number
MKCK8390
MKBZ1304V
MKBS0626V
MKBH9337V
94996LJ

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Staudinger ligation: a new immobilization strategy for the preparation of small-molecule arrays.
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Angewandte Chemie (International ed. in English), 42(47), 5830-5834 (2003-12-16)
Covalent modification of carbon nanotubes with anthraquinone by electrochemical grafting and solid phase synthesis.
Ghanem MA, et al.
Electrochimica Acta, 68, 74-80 (2012)
Sven W Meckelmann et al.
Prostaglandins & other lipid mediators, 130, 8-15 (2017-02-22)
The performance of two derivatization and ionization techniques for the quantitative reversed phase liquid chromatography (LC)- mass spectrometry (MS) analysis of hydroxy fatty acids (OH-PUFA) in plasma was evaluated: One used AMPP (N-(4-aminomethylphenyl)pyridinium chloride) leading to a positive charged amid-derivate
László Szabó et al.
Materials (Basel, Switzerland), 12(1) (2019-01-10)
While intensive efforts are made to prepare carbon fiber reinforced plastics from renewable sources, less emphasis is directed towards elaborating green approaches for carbon fiber surface modification to improve the interfacial adhesion in these composites. In this study, we covalently

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