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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.)

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 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

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

450359-25G:
450359-BULK:
450359-VAR:

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Certificates of Analysis (COA)

Lot/Batch Number
MKBZ7855V
MKBN8155V
MKBH2137V
MKBB6785
04025DJ

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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)
Catalyst-free water-mediated N-Boc deprotection.
Wang G, et al.
Tetrahedron Letters, 50(13), 1438-1440 (2009)
Novel practical deprotection of N-Boc compounds using fluorinated alcohols.
Choy J, et al.
Synthetic Communications, 38(21), 3840-3853 (2008)
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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