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化驗
97%
折射率
n20/D 1.49 (lit.)
bp
265 °C (lit.)
密度
0.912 g/mL at 25 °C (lit.)
SMILES 字串
CN(C1CCCCC1)C2CCCCC2
InChI
1S/C13H25N/c1-14(12-8-4-2-5-9-12)13-10-6-3-7-11-13/h12-13H,2-11H2,1H3
InChI 密鑰
GSCCALZHGUWNJW-UHFFFAOYSA-N
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應用
N,N -二环己基甲胺的用途如下:
- 叔醇与有机铋 (V) 化合物 O 苯基化反应中的催化剂
- 1-(o-溴苯基)-2-甲基脯氨酸-2-烯-1-醇在钯催化下 5-内三角环化反应中的碱
訊號詞
Danger
危險聲明
危險分類
Acute Tox. 4 Oral - Skin Corr. 1B
儲存類別代碼
8A - Combustible corrosive hazardous materials
水污染物質分類(WGK)
WGK 2
閃點(°F)
230.0 °F - closed cup
閃點(°C)
110 °C - closed cup
個人防護裝備
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
Nature communications, 11(1), 2960-2960 (2020-06-13)
Nucleic acid-based materials enable sub-nanometer precision in self-assembly for fields including biophysics, diagnostics, therapeutics, photonics, and nanofabrication. However, structural DNA nanotechnology has been limited to substantially hydrated media. Transfer to organic solvents commonly used in polymer and peptide synthesis results
Copper (II)-catalyzed O-phenylation of alcohols with organobismuth (V) reagents.
ARKIVOC (Gainesville, FL, United States), 7, 254-264 (2007)
Heck-type reactions of allylic alcohols: Part IV:(2-Substituted)-1-indanones via 5-endo-trig cyclizations.
J. Mol. Catal. A: Chem., 283(1), 140-145 (2008)
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