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450359

Sigma-Aldrich

N-Boc-aniline

97%

Synonym(s):

tert-Butyl-N-phenylcarbamate

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About This Item

Linear Formula:
C6H5NHCO2C(CH3)3
CAS Number:
3422-01-3
Molecular Weight:
193.24
MDL number:
MFCD00043723
UNSPSC Code:
12352100
PubChem Substance ID:
24868240
NACRES:
NA.22

Quality Level

100

Assay

97%

mp

133-137 °C (lit.)

SMILES string

CC(C)(C)OC(=O)Nc1ccccc1

InChI

1S/C11H15NO2/c1-11(2,3)14-10(13)12-9-7-5-4-6-8-9/h4-8H,1-3H3,(H,12,13)

InChI key

KZZHPWMVEVZEFG-UHFFFAOYSA-N

Related Categories

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

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Directed ortho lithiation of phenylcarbamic acid 1, 1-dimethylethyl ester (N-BOC-aniline). Revision and improvements.
Stanetty P, et al.
The Journal of Organic Chemistry, 57(25), 6833-6837 (1992)
Novel practical deprotection of N-Boc compounds using fluorinated alcohols.
Choy J, et al.
Synthetic Communications, 38(21), 3840-3853 (2008)
SNAr reactions of benzaldimines: a concise synthesis of substituted phenanthridines.
Reuter DC, et al.
Tetrahedron Letters, 35(28), 4899-4902 (1994)
Total synthesis of the polycyclic fungal metabolite (+/-)-communesin F.
Peng Liu et al.
Angewandte Chemie (International ed. in English), 49(11), 2000-2003 (2010-02-23)
Catalyst-free water-mediated N-Boc deprotection.
Wang G, et al.
Tetrahedron Letters, 50(13), 1438-1440 (2009)

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