(2S)-3-[4-({[(2,2-Dichloroethenyl)oxy]sulfonyl}oxy)phenyl]-Fmoc-2-aminopropanoic acid

This compound is a protected amino acid derivative containing an Fmoc group and a dichloroethenyl-sulfonyl-modified aromatic ring. The steric and electronic features support incorporation into specialized peptidomimetics. Researchers employ it to study reactivity, coupling efficiency, and structural constraints. Its custom side chain enables design of rigid or electrophilic peptide frameworks.

Designed for biological research and industrial applications, not intended for individual clinical or medical purposes.
(2S)-3-[4-({[(2,2-Dichloroethenyl)oxy]sulfonyl}oxy)phenyl]-Fmoc-2-aminopropanoic acid(CAS 1151854-06-6)

CAT No: 10-101-286

CAS No:1151854-06-6

Synonyms/Alias:FMOC-L-TYR(SO3DCV)-OH;1151854-06-6;MFCD26408195;E70910;(2S)-3-[4-(([(2,2-Dichloroethenyl)oxy]sulfonyl)oxy)phenyl]-fmoc-2-aminopropanoic acid;(2S)-3-[4-(2,2-dichloroethenoxysulfonyloxy)phenyl]-2-(9H-fluoren-9-ylmethoxycarbonylamino)propanoic acid;

Custom Peptide Synthesis
cGMP Peptide
  • Registration of APIs
  • CMC information required for an IND
  • IND and NDA support
  • Drug master files (DMF) filing
M.F/Formula
C26H21Cl2NO8S
M.W/Mr.
578.4
Purity
>98 %
Source#
Synthetic
Shipping Condition
Room temperature
InChI
InChI=1S/C26H21Cl2NO8S/c27-24(28)15-36-38(33,34)37-17-11-9-16(10-12-17)13-23(25(30)31)29-26(32)35-14-22-20-7-3-1-5-18(20)19-6-2-4-8-21(19)22/h1-12,15,22-23H,13-14H2,(H,29,32)(H,30,31)/t23-/m0/s1
InChI Key
JDNCIOFMCRYUMK-QHCPKHFHSA-N

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