450359
N-Boc-aniline
97%
Synonym(s):
tert-Butyl-N-phenylcarbamate
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About This Item
Linear Formula:
C6H5NHCO2C(CH3)3
CAS Number:
Molecular Weight:
193.24
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Product Name
N-Boc-aniline, 97%
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)
SMILES string
CC(C)(C)OC(=O)Nc1ccccc1
InChI key
KZZHPWMVEVZEFG-UHFFFAOYSA-N
assay
97%
mp
133-137 °C (lit.)
functional group
amine
Quality Level
Related Categories
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Novel practical deprotection of N-Boc compounds using fluorinated alcohols.
Choy J, et al.
Synthetic Communications, 38(21), 3840-3853 (2008)
Catalyst-free water-mediated N-Boc deprotection.
Wang G, et al.
Tetrahedron Letters, 50(13), 1438-1440 (2009)
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)
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)
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