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
CAS Number:
分子量:
275.34
Beilstein:
4454820
MDL编号:
UNSPSC代码:
12352209
PubChem化学物质编号:
NACRES:
NA.22
Product Name
Boc-Thr(tBu)-OH,
方案
95%
质量水平
表单
powder
mp
98.9 °C
应用
peptide synthesis
储存温度
2-8°C
SMILES字符串
C[C@@H](OC(C)(C)C)[C@H](NC(=O)OC(C)(C)C)C(O)=O
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
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一般描述
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.
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
法规信息
新产品
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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