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15390

Sigma-Aldrich

Boc-Ser(Bzl)-OH

≥99.0% (T)

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Synonym(s):
N-(tert-Butoxycarbonyl)-O-benzyl-L-serine, Boc-O-benzyl-L-serine
Linear Formula:
C6H5CH2OCH2CH(COOH)NHCOOC(CH3)3
CAS Number:
Molecular Weight:
295.33
Beilstein:
3064461
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

≥99.0% (T)

form

solid

optical activity

[α]20/D +20±1°, c = 2% in ethanol: water (4:1)

reaction suitability

reaction type: Boc solid-phase peptide synthesis

mp

58-60 °C (lit.)

application(s)

peptide synthesis

SMILES string

CC(C)(C)OC(=O)N[C@@H](COCc1ccccc1)C(O)=O

InChI

1S/C15H21NO5/c1-15(2,3)21-14(19)16-12(13(17)18)10-20-9-11-7-5-4-6-8-11/h4-8,12H,9-10H2,1-3H3,(H,16,19)(H,17,18)/t12-/m0/s1

InChI key

DMBKPDOAQVGTST-LBPRGKRZSA-N

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1 of 4

This Item
1507841048915490
Boc-Ser(Bzl)-OH ≥99.0% (T)

Sigma-Aldrich

15390

Boc-Ser(Bzl)-OH

Boc-D-Ser(Bzl)-OH ≥98.0% (HPLC)

Sigma-Aldrich

15078

Boc-D-Ser(Bzl)-OH

Boc-Ser-OMe 95%

Sigma-Aldrich

410489

Boc-Ser-OMe

Boc-Pro-OH ≥99.0% (T)

Sigma-Aldrich

15490

Boc-Pro-OH

form

solid

form

-

form

liquid

form

solid

optical activity

[α]20/D +20±1°, c = 2% in ethanol: water (4:1)

optical activity

-

optical activity

[α]20/D −18°, c = 5 in methanol

optical activity

[α]20/D −61±2°, c = 2% in acetic acid

mp

58-60 °C (lit.)

mp

-

mp

-

mp

133-135 °C (lit.)

Quality Level

100

Quality Level

100

Quality Level

-

Quality Level

100

reaction suitability

reaction type: Boc solid-phase peptide synthesis

reaction suitability

reaction type: Boc solid-phase peptide synthesis

reaction suitability

reaction type: Boc solid-phase peptide synthesis

reaction suitability

reaction type: Boc solid-phase peptide synthesis

Storage Class Code

11 - 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

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Huang-Han Chen et al.
Analytica chimica acta, 865, 53-59 (2015-03-04)
Polydimethylsiloxane (PDMS) is widely used for microfabrication and bioanalysis; however, its surface functionalization is limited due to the lack of active functional groups and incompatibility with many solvents. We presented a novel approach for in situ fabrication of cleavable peptide

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