2'-O-(2-Methoxyethyl)cytidine

 化学構造式
223777-16-0
CAS番号.
223777-16-0
化学名:
别名:
英語名:
2'-O-(2-Methoxyethyl)cytidine
英語别名:
2'-MOE-C;2'-MOE-rC;2'-O-MOE-rC;2'-O-MOE-Cr;2'-MOE-Cytidine;2'-O-MOE Cytidine;2'-O-MOE Cytidine;2'-O-(2-mthoxyethyl)Cytidine;2'-O-(2-Methoxyethyl)cytidine;2'-O-(2-Methoxyethyl)cytidine
CBNumber:
CB32510559
化学式:
C12H19N3O6
分子量:
301.3
MOL File:
223777-16-0.mol

2'-O-(2-Methoxyethyl)cytidine 物理性質

沸点 :
535.3±60.0 °C(Predicted)
比重(密度) :
1.57±0.1 g/cm3(Predicted)
貯蔵温度 :
2-8°C
溶解性:
DMSO : 250 mg/mL (829.74 mM)
酸解離定数(Pka):
13.36±0.70(Predicted)
外見 :
Solid
色:
White to off-white
InChI:
InChI=1S/C12H19N3O6/c1-19-4-5-20-10-9(17)7(6-16)21-11(10)15-3-2-8(13)14-12(15)18/h2-3,7,9-11,16-17H,4-6H2,1H3,(H2,13,14,18)/t7-,9-,10-,11-/m1/s1
InChIKey:
YKOGMMXZKKVMBT-QCNRFFRDSA-N
SMILES:
OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](OCCOC)[C@@H]1O
安全性情報
  • リスクと安全性に関する声明
  • 危険有害性情報のコード(GHS)
絵表示(GHS) GHS hazard pictograms
注意喚起語 警告
危険有害性情報
コード 危険有害性情報 危険有害性クラス 区分 注意喚起語 シンボル P コード
H302 飲み込むと有害 急性毒性、経口 4 警告 GHS hazard pictograms P264, P270, P301+P312, P330, P501
H315 皮膚刺激 皮膚腐食性/刺激性 2 警告 GHS hazard pictograms P264, P280, P302+P352, P321,P332+P313, P362
H319 強い眼刺激 眼に対する重篤な損傷性/眼刺激 性 2A 警告 GHS hazard pictograms P264, P280, P305+P351+P338,P337+P313P
H335 呼吸器への刺激のおそれ 特定標的臓器毒性、単回暴露; 気道刺激性 3 警告 GHS hazard pictograms
注意書き
P261 粉じん/煙/ガス/ミスト/蒸気/スプレーの吸入を避ける こと。
P305+P351+P338 眼に入った場合:水で数分間注意深く洗うこと。次にコ ンタクトレンズを着用していて容易に外せる場合は外す こと。その後も洗浄を続けること。

2'-O-(2-Methoxyethyl)cytidine 価格

メーカー 製品番号 製品説明 CAS番号 包装 価格 更新時間 購入

2'-O-(2-Methoxyethyl)cytidine 化学特性,用途語,生産方法

使用

A cytidine derivative as building blocks for cross-linking oligonucleotides.

合成

2'-O-(2-Methoxyethyl)uridine could be converted into the corresponding cytidine derivative (2'-O-(2-Methoxyethyl)cytidine) by the 4-nitrophenylation[1]. 2'-O-(2-Methoxyethyl)uridine, l-methylpyrrolidine, chlorotrimethylsilane and dry acetonitrile were stirred together at rt. After 1 h, the reaction mixture was cooled to 0 ℃, and trifluoroacetic anhydride was added dropwise over 5 min. After a further period of 30 rain at 0 ℃, 4-nitrophenol was added to the stirred reactants which were maintained at 0 °C. After 3 h, the products were poured into saturated aqueous sodium hydrogen carbonate, and the resulting mixture was extracted with dichloromethane. The combined organic layers were dried, and evaporated under reduced pressure. Concentrated aqueous ammonia was added to a stirred solution of the residue in dioxane, contained in a sealed flask that was then heated at 55°C for 24 h. The resulting yellow solution was concentrated under reduced pressure and the residue was evaporated with absolute ethanol. The products were fractionated by short column chromatography on silica gel and were evaporated under reduced pressure to give 2'-O-(2-Methoxyethyl)cytidine as an off-white solid.
説明図

2'-O-(2-Methoxyethyl)cytidine 上流と下流の製品情報

原材料

準備製品


2'-O-(2-Methoxyethyl)cytidine 生産企業

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223777-16-0()キーワード:


  • 223777-16-0
  • 2'-O-(2-Methoxyethyl)cytidine
  • 2'-O-MOE Cytidine
  • 4-AMINO-1-[(2R,3R,4R,5R)-4-HYDROXY-5-(HYDROXYMETHYL)-3-(2-METHOXYETHOXY)OXOLAN-2-YL]PYRIMIDIN-2-ONE
  • 2'-O-(2-Methoxyethyl)-cytidine, >97%
  • 4-AMINO-1-[4-HYDROXY-5-(HYDROXYMETHYL)-3-(2-METHOXYETHOXY)OXOLAN-2-YL]PYRIMIDIN-2-ONE
  • 4-amino-1-[(2R,3S,4S,5R)-4-hydroxy-5-(hydroxymethyl)-3-(2-methoxyethoxy)tetrahydrofuran-2-yl]pyrimidin-2-one
  • Cytidine, 2'-O-(2-methoxyethyl)-
  • 2'-O-MOE-rC
  • 2'-MOE-Cytidine
  • 2'-O-MOE-Cr
  • 2'-MOE-rC
  • 2'-MOE-C
  • 4-amino-1-[(2R,3R,4R,5R)-4-hydroxy-5-(hydroxymethyl)-3-(2-methoxyethoxy)tetrahydrofuran-2-yl]pyrimidin-2-one
  • 2'-O-(2-mthoxyethyl)Cytidine
  • 2'-O-(2-Methoxyethyl)cytidine
  • 2'-O-MOE Cytidine
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