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CAS RN: 93183-36-9 | 產品號碼: D6204

Diisopropylammonium Tetrazol-1-ide


纯度/分析方法: >98.0%(T)(HPLC)
別名
  • Diisopropylammonium Tetrazolide
文件:
5G
NT$3,640
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25G
NT$12,320
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* TCI會時常優化儲存條件,儲存溫度請以在線目錄為準,敬請留意。


產品號碼 D6204
純度/分析方法 >98.0%(T)(HPLC)
分子式 / 分子量 C__6H__1__5N·CH__2N__4 = 171.25 
外觀與形狀(20°C) Solid
儲存條件 Refrigerated (0-10°C)
儲存在惰性氣體下 Store under inert gas
應避免的情況 Air Sensitive,Hygroscopic,Heat Sensitive
包裝和容器 5G-Glass Bottle with Plastic Insert (閲覽圖片)
CAS RN 93183-36-9
Reaxys-RN 3569216
產品規格
Appearance White to Light yellow powder to crystal
Purity(HPLC) min. 98.0 area%
Purity(Nonaqueous Titration) min. 98.0 %
Melting point 150.0 to 154.0 °C
NMR confirm to structure
性質
熔點 152 °C
GHS
圖形表示 Pictogram
信號詞 Warning
危險性說明 H315 : Causes skin irritation.
H319 : Causes serious eye irritation.
防範說明 P264 : Wash skin thoroughly after handling.
P280 : Wear protective gloves/ eye protection/ face protection.
P302 + P352 : IF ON SKIN: Wash with plenty of water.
P337 + P313 : If eye irritation persists: Get medical advice/ attention.
P305 + P351 + P338 : IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing.
P362 + P364 : Take off contaminated clothing and wash it before reuse.
P332 + P313 : If skin irritation occurs: Get medical advice/ attention.
相關法規
運輸資料
HS編碼* 2933.99-000
*此H.S.編碼用於日本出口報關, 不適用於您所在國家或地區的進口申報
Application
TCI Practical Example: Phosphoroamidite Synthesis Using Diisopropylammonium Tetrazole

 TCI Practical Example: Phosphoroamidite Synthesis Using Diisopropylammonium Tetrazole

Used Chemicals

Procedure

2-Cyanoethyl N,N,N',N'-tetraisopropylphosphorodiamidite (0.7 mL, 2.2 mmol, 1.2 eq.) was added to a solution of DMT-T (1.0 g, 1.8 mmol) and diisopropylammonium tetrazole (160 mg, 0.92 mmol, 0.5 eq.) in dichloromethane (9.2 mL) at room temperature. After the completion of the reaction, saturated aq. NaHCO3 (5 mL) was added to the solution and extracted with dichloromethane (15 mL, twice). The organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure. The crude product was purified by silica gel column chromatography (hexane:ethyl acetate = 70:30 - 50:50, 2% of triethylamine was added to the eluents) to give 1 (1.2 g, 88% yield) as a white crystal.

Experimenter’s Comments

The reaction solution was monitored by NMR.

Analytical Data

Compound 1

1H NMR (400 MHz, CDCl3); δ 11.36 (s, 1H), 7.50 (d, J = 4.0 Hz, 1H), 7.36-7.20 (m, 9H), 6.87-6.83 (m, 4H), 6.16-6.15 (m, 1H), 4.56-4.49 (m, 1H), 3.99 (d, J = 4.0 Hz, 1H), 3.73-3.72 (m, 1H), 3.22-3.19 (m, 1H), 2.72 (t, J = 8.0 Hz, 1H), 2.62 (t, J = 1.2 Hz, 1H), 2.41-2.31 (m, 1H), 1.44 (d, J = 1.2 Hz, 3H), 1.18-1.06 (m, 12H).

Lead Reference

Other Reference


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