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450359

Sigma-Aldrich

N-Boc-aniline

97%

Synonym(s):

tert-Butyl-N-phenylcarbamate

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25 G
$150.10

$150.10

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25 G
$150.10

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

$150.10

List Price$158.00Save 5%
Web-Only Promotion

Available to ship onApril 29, 2025Details

Request a Bulk Order

Quality Level

100

assay

97%

mp

133-137 °C (lit.)

functional group

amine

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

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Certificates of Analysis (COA)

Lot/Batch Number
MKCR6403
MKBZ7855V
MKBN8155V
MKBH2137V
MKBB6785

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SNAr reactions of benzaldimines: a concise synthesis of substituted phenanthridines.
Reuter DC, et al.
Tetrahedron Letters, 35(28), 4899-4902 (1994)
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)
Catalyst-free water-mediated N-Boc deprotection.
Wang G, et al.
Tetrahedron Letters, 50(13), 1438-1440 (2009)
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)

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