Skip to Content
Merck
All Photos(1)

Documents

189855

Sigma-Aldrich

2,3-Dimethoxybenzylamine

99%

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
(CH3O)2C6H3CH2NH2
CAS Number:
Molecular Weight:
167.21
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:

Assay

99%

form

solid

refractive index

n20/D 1.54 (lit.)

bp

137 °C/11 mmHg (lit.)

density

1.13 g/mL at 25 °C (lit.)

SMILES string

COc1cccc(CN)c1OC

InChI

1S/C9H13NO2/c1-11-8-5-3-4-7(6-10)9(8)12-2/h3-5H,6,10H2,1-2H3

InChI key

LVMPWFJVYMXSNY-UHFFFAOYSA-N

Application

2,3-Dimethoxybenzylamine was used in the synthesis of di-,tri- and tetrapeptide linked dicatechol derivatives and 1-aryl-2,3-dihydro-1H-isoindoles (isoindolines).

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

235.4 °F - closed cup

Flash Point(C)

113 °C - closed cup

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

Di-, Tri-and tetrapeptide-linked dicatechol derivatives.
Albrecht M, et al.
Synthesis, 2002, 126-132 null
Facile synthesis of 1-aryl-2, 3-dihydro-1H-isoindoles by cyclization of N-formyliminium ion via geometrically disfavored 5-endo-trig process.
Kitabatake M, et al.
Heterocycles, 78(5), 1177-1181 (2009)

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