推荐产品
质量水平
方案
≥99.0% (HPLC)
反应适用性
reaction type: Coupling Reactions
mp
140 °C (dec.) (lit.)
应用
peptide synthesis
官能团
amine
储存温度
2-8°C
SMILES字符串
F[B-](F)(F)F.CN(C)C(\ON1C=CC=CC1=O)=[N+](/C)C
InChI
1S/C10H16N3O2.BF4/c1-11(2)10(12(3)4)15-13-8-6-5-7-9(13)14;2-1(3,4)5/h5-8H,1-4H3;/q+1;-1
InChI key
CZQGINAUZYECAI-UHFFFAOYSA-N
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应用
Reagent for:
Amidation
Peptide Coupling
Esterification of nucleosides to solid phase supports for oligonucleoside synthesis
Amidation
Peptide Coupling
Esterification of nucleosides to solid phase supports for oligonucleoside synthesis
其他说明
多肽合成的偶联剂，特别适合于无外消旋作用的片段缩合反应
警示用语：
Danger
危险声明
危险分类
Eye Dam. 1 - Skin Sens. 1A
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
法规信息
新产品
R T Pon et al.
Bioconjugate chemistry, 10(6), 1051-1057 (1999-11-24)
Nucleosides can be esterified to solid-phase supports using uronium or phosphonium coupling reagents and a coupling additive, such as 1-hydroxybenzotriazole (HOBT), 7-aza-1-hydroxybenzotriazole (HOAT), N-methylimidazole (NMI), or 4-(dimethylamino)pyridine (DMAP). However, DMAP was far superior to other additives and high nucleoside loadings
C M Huntley et al.
Nucleosides, nucleotides & nucleic acids, 20(4-7), 731-733 (2001-09-21)
The synthesis of 1-(beta-D-ribofuranosyl)pyridin-2-one-3-carboxylic acid and the 3-carboxamide as well as a short series of 3N-carboxamides, prepared by TPTU/HOBt coupling of primary amines with 1-(beta-D-ribofuranosyl)pyridin-2-one-3-carboxylic acid, and their evaluation as anti-infective agents is described.
Tomohisa Sawada et al.
Journal of the American Chemical Society, 133(19), 7336-7339 (2011-04-28)
Artificial mimicry of α-helices offers a basis for development of protein-protein interaction antagonists. Here we report a new type of unnatural peptidic backbone, containing α-, β-, and γ-amino acid residues in an αγααβα repeat pattern, for this purpose. This unnatural
Knorr, R, et al.
Tetrahedron Letters, 30, 1927-1927 (1989)
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