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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 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

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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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