909505
C8-Alkyne-dU-CEP
동의어(들):
5-(Octa-1,7-diynyl)-3′-O-[(2-cyanoethoxy)(diisopropylamino)-phosphono)]-5′-O- (4,4′-dimethoxytrityl)-2′-deoxyuridine, 5-Octadiynyl-dU CEP, C8-Alkyne dU phosphoramidite
로그인조직 및 계약 가격 보기
모든 사진(2)
About This Item
실험식(Hill 표기법):
C47H55N4O8P
CAS Number:
Molecular Weight:
834.94
MDL number:
UNSPSC 코드:
41116105
NACRES:
NA.22
추천 제품
![Tris[(1-benzyl-1H-1,2,3-triazol-4-yl)methyl]amine 97%](/deepweb/assets/sigmaaldrich/product/structures/179/695/86a721c8-2a4c-4e4f-bc36-6276ce7a941f/640/86a721c8-2a4c-4e4f-bc36-6276ce7a941f.png)
![3-Bromo-1H-pyrazolo[3,4-d]pyrimidin-4-amine AldrichCPR](/deepweb/assets/sigmaaldrich/product/structures/794/777/0edc2115-9a26-4d94-8c55-80a2d58bdae7/640/0edc2115-9a26-4d94-8c55-80a2d58bdae7.png)
양식
powder
반응 적합성
reaction type: click chemistry
저장 온도
−20°C
SMILES string
P(N(C(C)C)C(C)C)(OC1[C@H](O[C@H](C1)N2C=C(C(=O)NC2=O)C#CCCCCC#C)COC([3H])[2H])OCCC#N
InChI
1S/C27H39N4O6P/c1-7-8-9-10-11-12-14-22-18-30(27(33)29-26(22)32)25-17-23(24(36-25)19-34-6)37-38(35-16-13-15-28)31(20(2)3)21(4)5/h1,18,20-21,23-25H,8-11,13,16-17,19H2,2-6H3,(H,29,32,33)/t23?,24-,25-,38?/m1/s1/i6TD/t6?,23?,24-,25-,38?
InChI key
VMEOYXBOBQPPSL-YSJOBRKDSA-N
애플리케이션
This functional phosphoramidite is used to introduce click handles univerally (5′ internal and 3′end) into oligonucleotides under standard conditions for solid phase synthesis. Afterwards the oligonucleotide (RNA, PNA, DNA) can be efficiently conjugated using a copper-catalyzed click reaction to azide-functionalized moieties such as fluorescent dye azides and azido amino acids
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
가장 최신 버전 중 하나를 선택하세요:
Frank Seela et al.
Chemistry & biodiversity, 3(5), 509-514 (2006-12-29)
The synthesis of a series of oligonucleotides containing 5-substituted pyrimidines as well as 7-substituted 7-deazapurines bearing diyne groups with terminal triple bonds is reported. The modified nucleosides were prepared from the corresponding iodo nucleosides and diynes by the Sonogashira cross-coupling
DNA photography: an ultrasensitive DNA-detection method based on photographic techniques.
David M Hammond et al.
Angewandte Chemie (International ed. in English), 46(22), 4184-4187 (2007-04-27)
Dorota I Rozkiewicz et al.
Chembiochem : a European journal of chemical biology, 8(16), 1997-2002 (2007-09-15)
This paper describes a straightforward procedure to immobilize oligonucleotides on glass substrates in well-defined micropatterns by microcontact printing with a dendrimer-modified stamp. The oligonucleotides are efficiently immobilized by "click" chemistry induced by microcontact printing. Acetylene-modified oligonucleotides were treated with an
Johannes Gierlich et al.
Organic letters, 8(17), 3639-3642 (2006-08-11)
[reaction: see text] We report the development of the Cu(I)-catalyzed Huisgen cycloaddition (click) reaction for the multiple postsynthetic labeling of alkyne-modified DNA. A series of alkyne-modified oligodeoxyribonucleotides (ODNs) of increasing alkyne density were prepared, and the click reaction using various
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