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About This Item
Empirical Formula (Hill Notation):
C9H17NO5
CAS Number:
Molecular Weight:
219.23
MDL number:
UNSPSC Code:
12352209
PubChem Substance ID:
NACRES:
NA.26
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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 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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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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