Skip to Content
Merck
CN

47565

Fmoc-Tyr(Bzl)-OH

≥98.0% (HPLC)

Synonym(s):

Fmoc-O-benzyl-L-tyrosine

Sign In to View Organizational & Contract Pricing.

Select a Size

About This Item

Empirical Formula (Hill Notation):
C31H27NO5
CAS Number:
71989-40-7
Molecular Weight:
493.55
PubChem Substance ID:
57651013
UNSPSC Code:
12352200
Beilstein/REAXYS Number:
4341195
MDL number:
MFCD00065682

Key Documents

View All Documentation
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

Product Name

Fmoc-Tyr(Bzl)-OH, ≥98.0% (HPLC)

SMILES string

OC(=O)[C@H](Cc1ccc(OCc2ccccc2)cc1)NC(=O)OCC3c4ccccc4-c5ccccc35

InChI

1S/C31H27NO5/c33-30(34)29(18-21-14-16-23(17-15-21)36-19-22-8-2-1-3-9-22)32-31(35)37-20-28-26-12-6-4-10-24(26)25-11-5-7-13-27(25)28/h1-17,28-29H,18-20H2,(H,32,35)(H,33,34)/t29-/m0/s1

InChI key

REHSJSKPWIOKIJ-LJAQVGFWSA-N

assay

≥98.0% (HPLC)

optical activity

[α]20/D −16.0±2.5°, c = 1% in DMF

mp

157-161 °C

application(s)

peptide synthesis

functional group

Fmoc

storage temp.

2-8°C

Storage Class

13 - Non Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Regulatory Information

新产品
This item has

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
BCBP1610V
BCBF4514V
BCBG8442V
442064/1
430228/1

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.

Search for a COA

Already Own This Product?

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

Visit the Document Library

Chloé Guilbaud-Chéreau et al.
ACS applied materials & interfaces, 11(14), 13147-13157 (2019-03-14)
Molecular gels formed by the self-assembly of low-molecular-weight gelators have received increasing interest because of their potential applications in drug delivery. In particular, the ability of peptides and amino acids to spontaneously self-assemble into three-dimensional fibrous network has been exploited

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