15500
Boc-Ser-OH
≥99.0% (T), for peptide synthesis
Synonym(s):
N-(tert-Butoxycarbonyl)-L-serine, Boc-L-serine
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About This Item
Linear Formula:
HOCH2CH(COOH)NHCOOC(CH3)3
CAS Number:
Molecular Weight:
205.21
NACRES:
NA.22
PubChem Substance ID:
eCl@ss:
32160406
UNSPSC Code:
12352209
EC Number:
221-867-3
MDL number:
Beilstein/REAXYS Number:
2212252
Product Name
Boc-Ser-OH, ≥99.0% (T)
Quality Segment
assay
≥99.0% (T)
optical activity
[α]20/D −3.5±0.5°, c = 2% in acetic acid
reaction suitability
reaction type: Boc solid-phase peptide synthesis
mp
91 °C (dec.) (lit.)
application(s)
peptide synthesis
storage temp.
2-8°C
SMILES string
CC(C)(C)OC(=O)N[C@@H](CO)C(O)=O
InChI
1S/C8H15NO5/c1-8(2,3)14-7(13)9-5(4-10)6(11)12/h5,10H,4H2,1-3H3,(H,9,13)(H,11,12)/t5-/m0/s1
InChI key
FHOAKXBXYSJBGX-YFKPBYRVSA-N
General description
Boc-Ser-OH is an amino acid derivative.
Application
Boc-Ser-OH may be used in the synthesis of the following:
- 2-(N-Fmoc)-3-(N-Boc-N-methoxy)-diaminopropanoic acid (Fmoc: 9-fluorenylmethoxycarbonyl; Boc: t-butyloxycarbonyl)
- Boc-Ser-Leu-OMe
- cyclic peptide synthesis
- benzylsulfonyl-D-Ser-Ser-4-amidinobenzylamide
Building block in peptide synthesis. Starting material for the synthesis of various α-amino acids via the β-lactone.
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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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