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B4645

Sigma-Aldrich

Boc-Homoser-OH

>99%

Synonym(s):

Boc-L-homoserine

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About This Item

Empirical Formula (Hill Notation):
C9H17NO5
CAS Number:
41088-86-2
Molecular Weight:
219.23
MDL number:
MFCD00057839
UNSPSC Code:
12352209
PubChem Substance ID:
24891796
NACRES:
NA.26

product name

Boc-Homoser-OH,

assay

>99%

form

powder

color

white

application(s)

peptide synthesis

storage temp.

−20°C

SMILES string

CC(C)(C)OC(=O)NC(CCO)C(O)=O

InChI

1S/C9H17NO5/c1-9(2,3)15-8(14)10-6(4-5-11)7(12)13/h6,11H,4-5H2,1-3H3,(H,10,14)(H,12,13)

InChI key

PZEMWPDUXBZKJN-UHFFFAOYSA-N

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Biochem/physiol Actions

Boc-L-homoserine is N-terminal protected α amino acid used in organic synthesis of compounds such as the functionalizable methionine surrogate azidohomoalanine.

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Certificates of Analysis (COA)

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A James Link et al.
Nature protocols, 2(8), 1884-1887 (2007-08-19)
This protocol describes a synthetic route to the non-canonical amino acid azidohomoalanine (AHA) using protected homoserine as a starting material. An alternative route to AHA is presented in a companion paper. This synthesis can be completed in 5 days.

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