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15500

Boc-Ser-OH

Name: Boc-Ser-OH
Brand: ALDRICH

≥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:

3262-72-4

Molecular Weight:

205.21

NACRES:

NA.22

PubChem Substance ID:

57647375

eCl@ss:

32160406

UNSPSC Code:

12352209

EC Number:

221-867-3

MDL number:

MFCD00037243

Beilstein/REAXYS Number:

2212252

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Properties

Product Name

Boc-Ser-OH, ≥99.0% (T)

Quality Segment

100

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

Description

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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