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850489

L-Tyrosine methyl ester hydrochloride

Name: <SC>L</SC>-Tyrosine methyl ester hydrochloride
Brand: ALDRICH

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About This Item

Linear Formula:

HOC₆H₄CH₂CH(NH₂)COOCH₃ · HCl

CAS Number:

3417-91-2

Molecular Weight:

231.68

MDL number:

MFCD00012607

Beilstein/REAXYS Number:

3917353

NACRES:

NA.22

PubChem Substance ID:

24888297

eCl@ss:

32160406

UNSPSC Code:

12352209

EC Number:

222-313-3

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Properties

form

powder

Quality Level

200

optical activity

[α]25/D +74.0°, c = 3 in pyridine

reaction suitability

reaction type: solution phase peptide synthesis

mp

192 °C (dec.) (lit.)

application(s)

peptide synthesis

storage temp.

2-8°C

SMILES string

Cl.COC(=O)[C@@H](N)Cc1ccc(O)cc1

InChI

1S/C10H13NO3.ClH/c1-14-10(13)9(11)6-7-2-4-8(12)5-3-7;/h2-5,9,12H,6,11H2,1H3;1H/t9-;/m0./s1

InChI key

VXYFARNRGZWHTJ-FVGYRXGTSA-N

Description

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Helicity: A Non-Conventional Stereogenic Element for Designing Inherently Chiral Ionic Liquids for Electrochemical Enantiodifferentiation.

Francesca Fontana et al.

Molecules (Basel, Switzerland), 26(2) (2021-01-14)

Configurationally stable 5-aza[6]helicene (1) was envisaged as a promising scaffold for non-conventional ionic liquids (IL)s. It was prepared, purified, and separated into enantiomers by preparative HPLC on a chiral stationary phase. Enantiomerically pure quaternary salts of 1 with appropriate counterions

Inhibition of 3,5,3'-triiodothyronine binding to its receptor in rat liver by protease inhibitors and substrates.

J Brtko et al.

Molecular and cellular endocrinology, 93(1), 81-86 (1993-05-01)

Various protease inhibitors (e.g. phenylmethanesulfonyl fluoride (PMSF), tosyl-phenylalanine chloromethyl ketone (TosPheCH2Cl)) and substrates (e.g., tosyl-arginine methyl ester (TosArgOMe), tryptophan methyl ester (TrpOMe)) inhibit the binding of adrenal and sex steroids to their cognate receptors (Hubbard and Kalimi (1985) Mol. Cell.

Sensitized photooxidation of Di- and tripeptides of tyrosine.

S Criado et al.

Photochemistry and photobiology, 68(4), 453-458 (1998-10-31)

This paper studies the dye-sensitized photooxidation of tyrosine (tyr) and tyr di- and tripeptides (tyr-tyr and tyr-tyr-tyr) mediated by singlet molecular oxygen (O2[1 delta g]) in alkaline media. Photooxidation quantum efficiencies (phi r) were obtained by determining the overall and

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Global Trade Item Number

SKU	GTIN
850489-25G	04061833015322