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47561

Fmoc-Trp(Boc)-OH

Name: Fmoc-Trp(Boc)-OH
Brand: ALDRICH

≥97.0% (HPLC), for peptide synthesis

Synonym(s):

N_α-Fmoc-N_(in)-Boc-L-tryptophan, N_(in)-Boc-N_α-Fmoc-L-tryptophan

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About This Item

Empirical Formula (Hill Notation):

C₃₁H₃₀N₂O₆

CAS Number:

143824-78-6

Molecular Weight:

526.58

UNSPSC Code:

12352209

eCl@ss:

32160406

PubChem Substance ID:

57651011

NACRES:

NA.26

Beilstein/REAXYS Number:

7698009

MDL number:

MFCD00153366

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Properties

Product Name

Fmoc-Trp(Boc)-OH, ≥97.0% (HPLC)

Quality Segment

100

assay

≥97.0% (HPLC)

form

solid

optical activity

[α]20/D −21±2°, c = 1% in DMF

reaction suitability

reaction type: Fmoc solid-phase peptide synthesis

application(s)

peptide synthesis

functional group

Boc, Fmoc

storage temp.

2-8°C

SMILES string

CC(C)(C)OC(=O)n1cc(C[C@H](NC(=O)OCC2c3ccccc3-c4ccccc24)C(O)=O)c5ccccc15

InChI

1S/C31H30N2O6/c1-31(2,3)39-30(37)33-17-19(20-10-8-9-15-27(20)33)16-26(28(34)35)32-29(36)38-18-25-23-13-6-4-11-21(23)22-12-5-7-14-24(22)25/h4-15,17,25-26H,16,18H2,1-3H3,(H,32,36)(H,34,35)/t26-/m0/s1

InChI key

ADOHASQZJSJZBT-SANMLTNESA-N

Description

Application

Fmoc-Trp(Boc)-OH can be used for the synthesis of analogs of glucagon-like peptide-1 (GLP-1) for the treatment of type 2 diabetes and various peptides by Fmoc solid phase peptide synthesis (SPPS).

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Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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