37347
O-(2-Oxo-1(2H)pyridyl)-N,N,N′,N′-tetramethyluronium tetrafluoroborate
≥99.0% (HPLC)
동의어(들):
O-(1,2-Dihydro-2-oxo-1-pyridyl)-N,N,N′-N′-tetramethyluronium tetrafluoroborate, TPTU
로그인조직 및 계약 가격 보기
모든 사진(1)
About This Item
실험식(Hill 표기법):
C10H16BF4N3O2
CAS Number:
Molecular Weight:
297.06
MDL number:
UNSPSC 코드:
12352005
PubChem Substance ID:
NACRES:
NA.22
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추천 제품
Quality Level
분석
≥99.0% (HPLC)
반응 적합성
reaction type: Coupling Reactions
mp
140 °C (dec.) (lit.)
응용 분야
peptide synthesis
작용기
amine
저장 온도
2-8°C
SMILES string
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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신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Eye Dam. 1 - Skin Sens. 1A
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
개인 보호 장비
dust mask type N95 (US), Eyeshields, Gloves
이미 열람한 고객
![COMU 1-[(1-(Cyano-2-ethoxy-2-oxoethylideneaminooxy) dimethylaminomorpholino)] uronium hexafluorophosphate Novabiochem®](/deepweb/assets/sigmaaldrich/product/images/237/337/13566c06-8931-4cc2-8621-c8742a392cd6/640/13566c06-8931-4cc2-8621-c8742a392cd6.jpg)
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)
활성 필터
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