15504
Boc-Tic-OH
≥97.0% (TLC)
Synonym(s):
(S)-N-Boc-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid
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About This Item
Empirical Formula (Hill Notation):
C15H19NO4
CAS Number:
Molecular Weight:
277.32
PubChem Substance ID:
UNSPSC Code:
12352200
Beilstein/REAXYS Number:
4297114
MDL number:
assay
≥97.0% (TLC)
form
solid
optical activity
[α]20/D +19.0±1.5°, c = 0.7% in methanol
application(s)
peptide synthesis
storage temp.
2-8°C
SMILES string
CC(C)(C)OC(=O)N1Cc2ccccc2C[C@H]1C(O)=O
InChI
1S/C15H19NO4/c1-15(2,3)20-14(19)16-9-11-7-5-4-6-10(11)8-12(16)13(17)18/h4-7,12H,8-9H2,1-3H3,(H,17,18)/t12-/m0/s1
InChI key
HFPVZPNLMJDJFB-LBPRGKRZSA-N
Other Notes
Methylene-bridged derivative of BOC-L-phenylalanine.
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
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Yanchang Li et al.
Molecular cell, 76(1), 126-137 (2019-08-25)
A surprising complexity of ubiquitin signaling has emerged with identification of different ubiquitin chain topologies. However, mechanisms of how the diverse ubiquitin codes control biological processes remain poorly understood. Here, we use quantitative whole-proteome mass spectrometry to identify yeast proteins