Skip to Content
Merck
All Photos(1)

Key Documents

View All Documentation

Safety Information

681687

Sigma-Aldrich

N-Boc-1,2-phenylenediamine

95%

Synonym(s):

(2-Aminophenyl)-carbamic acid tert-butyl ester, Mono-N-Boc-o-phenylenediamine

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

About This Item

Empirical Formula (Hill Notation):
C11H16N2O2
CAS Number:
146651-75-4
Molecular Weight:
208.26
MDL number:
MFCD02169707
UNSPSC Code:
12352100
PubChem Substance ID:
24885650
NACRES:
NA.22

Assay

95%

form

solid

mp

109-114 °C

SMILES string

CC(C)(C)OC(=O)Nc1ccccc1N

InChI

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

InChI key

KCZFBLNQOSFGSH-UHFFFAOYSA-N

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H302,H317

Hazard Classifications

Acute Tox. 4 Oral - Skin Sens. 1

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

681687-BULK:
681687-250MG:
681687-VAR:
681687-1G:

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
05018TE

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

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

Visit the Document Library

Journal of the American Chemical Society, 115, 1321-1321 (1993)
Jonathan L Sessler et al.
Journal of the American Chemical Society, 127(32), 11442-11446 (2005-08-11)
The synthesis, characterization, and anion-binding properties of a series of 2,6-diamidopyridine dipyrromethane hybrid macrocycles is presented. As part of this work, a new method for effecting the oxidation of dipyrromethane-based macrocycles in organic solvents has been developed. The macrocyclic frameworks

Questions

Reviews

No rating value

Active Filters

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