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Safety Information

15504

Sigma-Aldrich

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:
78879-20-6
Molecular Weight:
277.32
Beilstein:
4297114
MDL number:
MFCD00143845
UNSPSC Code:
12352200
PubChem Substance ID:
57647378

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

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Other Notes

Methylene-bridged derivative of BOC-L-phenylalanine.

Storage Class Code

13 - Non Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
1387417V
1387417

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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

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