Skip to Content
Merck
All Photos(1)

Documents

53175

Sigma-Aldrich

N-Boc-m-phenylenediamine

≥98.0% (HPLC)

Synonym(s):

3-(tert-Butoxycarbonylamino)aniline, tert-Butyl-3-aminophenylcarbamate

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Empirical Formula (Hill Notation):
C11H16N2O2
CAS Number:
68621-88-5
Molecular Weight:
208.26
MDL number:
MFCD06657915
UNSPSC Code:
12352100
PubChem Substance ID:
57651399
NACRES:
NA.22

Assay

≥98.0% (HPLC)

reaction suitability

reagent type: cross-linking reagent

functional group

Boc
amine

SMILES string

NC1=CC(NC(OC(C)(C)C)=O)=CC=C1

InChI

1S/C11H16N2O2/c1-11(2,3)15-10(14)13-9-6-4-5-8(12)7-9/h4-7H,12H2,1-3H3,(H,13,14)

InChI key

IEUIEMIRUXSXCL-UHFFFAOYSA-N

Related Categories

Application

N-Boc-m-phenylenediamine (tert-Butyl-3-aminophenylcarbamate) may be used in the preparation of:
  • 5,5′-(propane-2,2-diyl)bis(N-(3-aminophenyl)-4-methyl-3-phenyl-1H-pyrrole-2-carboxamide)
  • ethyl 4-[{3-[(tert-butoxycarbonyl)amino]phenyl}amino]-2-chloropyrimidine-5-carboxylate
  • ethyl 4-(3-(tert-butoxycarbonyl)phenylamino)-2-(methylthio)pyrimidine-5-carboxylate

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H302

Precautionary Statements

P264 - P270 - P301 + P312 - P501

Hazard Classifications

Acute Tox. 4 Oral

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’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Design, synthesis, and biological evaluation of novel conformationally constrained inhibitors targeting epidermal growth factor receptor threonine790? methionine790 mutant.
Chang S, et al.
Journal of Medicinal Chemistry, 55(6), 2711-2723 (2012)
Pyrimido [4,5-d] pyrimidin-4(1H)-one Derivatives as Selective Inhibitors of EGFR Threonine790 to Methionine790 (T790M) Mutants.
Xu T, et al.
Angewandte Chemie (Weinheim an der Bergstrasse, Germany), 125(32), 8545-8548 (2013)
Grigory V Kolesnikov et al.
Organic & biomolecular chemistry, 9(21), 7358-7364 (2011-09-07)
The design and synthesis of a neutral macrocyclic host that is capable of perrhenate and pertechnetate recognition is described. The anion affinities and underlying coordination modes were estimated by several experimental and theoretical methods including a new technique--reverse (99)Tc NMR

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service