Skip to Content
Merck
All Photos(2)

Key Documents

472727

Sigma-Aldrich

3-(3,4-Dimethoxyphenyl)-L-alanine

97%, for peptide synthesis

Synonym(s):

(S)-2-Amino-3-(3,4-dimethoxyphenyl)propanoic acid, 3-Methoxy-O-methyl-L-tyrosine, DMPA

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
(CH3O)2C6H3CH2CH(NH2)CO2H
CAS Number:
Molecular Weight:
225.24
MDL number:
UNSPSC Code:
12352209
eCl@ss:
32160406
PubChem Substance ID:
NACRES:
NA.22

product name

3-(3,4-Dimethoxyphenyl)-L-alanine, 97%

Quality Level

Assay

97%

optical activity

[α]22/D −5°, c = 4 in 1 M HCl

reaction suitability

reaction type: solution phase peptide synthesis

mp

254-257 °C (lit.)

application(s)

peptide synthesis

SMILES string

COc1ccc(C[C@H](N)C(O)=O)cc1OC

InChI

1S/C11H15NO4/c1-15-9-4-3-7(6-10(9)16-2)5-8(12)11(13)14/h3-4,6,8H,5,12H2,1-2H3,(H,13,14)/t8-/m0/s1

InChI key

VWTFNYVAFGYEKI-QMMMGPOBSA-N

Application

3-(3,4-Dimethoxyphenyl)-L-alanine can be used as a reactant to synthesize (2S)-2-amino-3-[3,4-di(methoxy)phenyl]propan-1-ol (β-amino alcohol) for use as a key intermediate to prepare tetracyclic core of the Erythrina alkaloids.

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)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

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.

Already Own This Product?

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

Visit the Document Library

Facile and highly stereoselective synthesis of the tetracyclic erythrinane core
Allin SM, et al.
The Journal of Organic Chemistry, 67, 9464-9467 (2002)

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