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关于此项目
经验公式(希尔记法):
C47H55N4O8P
化学文摘社编号:
分子量:
834.94
MDL number:
UNSPSC Code:
41116105
NACRES:
NA.22
Form:
powder
form
powder
reaction suitability
reaction type: click chemistry
manufacturer/tradename
(BCA-03-1g)
storage temp.
−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
Application
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
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable