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189855

Sigma-Aldrich

2,3-Dimethoxybenzylamine

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

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

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

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.

FSL

Group 4: Flammable liquids
Type 3 petroleums
Hazardous rank III
Water insoluble liquid

JAN Code

189855-5G:
189855-BULK:
189855-VAR:
189855-25G:

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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