806501
Boc-Thr(tBu)-OH
95%, powder
别名:
N-叔丁氧羰基-O-叔丁基-L-苏氨酸
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关于此项目
线性分子式:
(CH3)3COCH(CH3)CH(COOH)NHCOOC(CH3)3
化学文摘社编号:
分子量:
275.34
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352209
MDL number:
Beilstein/REAXYS Number:
4454820
产品名称
Boc-Thr(tBu)-OH,
InChI
1S/C13H25NO5/c1-8(18-12(2,3)4)9(10(15)16)14-11(17)19-13(5,6)7/h8-9H,1-7H3,(H,14,17)(H,15,16)/t8-,9+/m1/s1
InChI key
LKRXXARJBFBMCE-BDAKNGLRSA-N
SMILES string
C[C@@H](OC(C)(C)C)[C@H](NC(=O)OC(C)(C)C)C(O)=O
assay
95%
form
powder
mp
98.9 °C
application(s)
peptide synthesis
storage temp.
2-8°C
Quality Level
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General description
Boc-Thr(t-Bu)-OH (N-Boc-O-tert-butyl-L-threonine) participates in the synthesis of 2,3-unsaturated glycosides, via reaction with per-O-acetylated glucal in the presence of Er(OTf)3 catalyst.
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
法规信息
新产品
此项目有
Antonio Procopio et al.
Carbohydrate research, 342(14), 2125-2131 (2007-06-23)
Er(OTf)(3) is a useful catalyst for the Ferrier rearrangement furnishing high yields of O- and S-glycosides. The transformation has wide applicability, cleaner reaction profiles, mild reaction conditions, and high stereoselectivity and the catalyst, which is also commercially available, can be
Christian Haenig et al.
Cell reports, 32(7), 108050-108050 (2020-08-20)
Interactome maps are valuable resources to elucidate protein function and disease mechanisms. Here, we report on an interactome map that focuses on neurodegenerative disease (ND), connects ∼5,000 human proteins via ∼30,000 candidate interactions and is generated by systematic yeast two-hybrid
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