Skip to Content
Merck
All Photos(1)

Documents

47311

Sigma-Aldrich

Fmoc-D-Ser(tBu)-OH

≥98.0% (TLC)

Synonym(s):

Fmoc-O-tert-butyl-D-serine

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C22H25NO5
CAS Number:
Molecular Weight:
383.44
Beilstein:
5309984
MDL number:
UNSPSC Code:
12352209
eCl@ss:
32160406
PubChem Substance ID:
NACRES:
NA.26

Quality Level

Assay

≥98.0% (TLC)

reaction suitability

reaction type: Fmoc solid-phase peptide synthesis

application(s)

peptide synthesis

functional group

Fmoc

storage temp.

2-8°C

SMILES string

CC(C)(C)OC[C@@H](NC(=O)OCC1c2ccccc2-c3ccccc13)C(O)=O

InChI

1S/C22H25NO5/c1-22(2,3)28-13-19(20(24)25)23-21(26)27-12-18-16-10-6-4-8-14(16)15-9-5-7-11-17(15)18/h4-11,18-19H,12-13H2,1-3H3,(H,23,26)(H,24,25)/t19-/m1/s1

InChI key

REITVGIIZHFVGU-LJQANCHMSA-N

related product

Product No.
Description
Pricing

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

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

Visit the Document Library

Customers Also Viewed

Slide 1 of 9

1 of 9

Fmoc-D-Phe-OH ≥98.0%

Sigma-Aldrich

47378

Fmoc-D-Phe-OH

Fmoc-D-Cys(Trt)-OH ≥97.0% (HPLC)

Sigma-Aldrich

08503

Fmoc-D-Cys(Trt)-OH

Fmoc-D-Glu(OtBu)-OH ≥98.0% (HPLC)

Sigma-Aldrich

07697

Fmoc-D-Glu(OtBu)-OH

Fmoc-D-Ile-OH ≥96.0% (HPLC)

Sigma-Aldrich

16905

Fmoc-D-Ile-OH

Fmoc-D-Lys(Boc)-OH 98%

Sigma-Aldrich

772054

Fmoc-D-Lys(Boc)-OH

Fmoc-D-Leu-OH ≥95.0% (TLC)

Sigma-Aldrich

47316

Fmoc-D-Leu-OH

Fmoc-His(Trt)-OH ≥98.0% (sum of enantiomers, HPLC)

Sigma-Aldrich

47639

Fmoc-His(Trt)-OH

Fmoc-Phe-OH 98%

Sigma-Aldrich

338338

Fmoc-Phe-OH

Fmoc-Gly-OH ≥98.0% (T)

Sigma-Aldrich

47627

Fmoc-Gly-OH

Fayçal Touti et al.
Nature chemical biology, 15(4), 410-418 (2019-03-20)
The use of competitive inhibitors to disrupt protein-protein interactions (PPIs) holds great promise for the treatment of disease. However, the discovery of high-affinity inhibitors can be a challenge. Here we report a platform for improving the affinity of peptide-based PPI
Andreas Pech et al.
Nucleic acids research, 45(7), 3997-4005 (2017-02-06)
Biological evolution resulted in a homochiral world in which nucleic acids consist exclusively of d-nucleotides and proteins made by ribosomal translation of l-amino acids. From the perspective of synthetic biology, however, particularly anabolic enzymes that could build the mirror-image counterparts

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