B4645
Boc-Homoser-OH
>99%
别名:
Boc-L-homoserine
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关于此项目
经验公式（希尔记法）:
C9H17NO5
化学文摘社编号:
分子量:
219.23
UNSPSC Code:
12352209
PubChem Substance ID:
NACRES:
NA.26
MDL number:
产品名称
Boc-Homoser-OH,
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
assay
>99%
form
powder
color
white
application(s)
peptide synthesis
storage temp.
−20°C
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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.
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
法规信息
新产品
此项目有
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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