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189855

2,3-Dimethoxybenzylamine

Name: 2,3-Dimethoxybenzylamine
Brand: ALDRICH

99%

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About This Item

Linear Formula:

(CH₃O)₂C₆H₃CH₂NH₂

CAS Number:

4393-09-3

Molecular Weight:

167.21

EC Number:

224-515-7

MDL number:

MFCD00052392

UNSPSC Code:

12352100

PubChem Substance ID:

24851401

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

GHS07

signalword

Warning

hcodes

H315,H319,H335

pcodes

P261 - P264 - P271 - P280 - P302 + P352 - P305 + P351 + P338

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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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)

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