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化驗
97%
形狀
liquid
折射率
n20/D 1.414 (lit.)
bp
140 °C (lit.)
密度
0.928 g/mL at 25 °C (lit.)
SMILES 字串
CNCC(OC)OC
InChI
1S/C5H13NO2/c1-6-4-5(7-2)8-3/h5-6H,4H2,1-3H3
InChI 密鑰
HUMIEJNVCICTPJ-UHFFFAOYSA-N
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應用
(Methylamino)acetaldehyde dimethyl acetal can be used as a reactant to synthesize:
- Aza[3.3.2] cyclazines by reacting with 5-methyloxazolo[3,2-a]pyridinium salts via synthesis of functionalized 5-aminoindolizines intermediates.
- N-(2,2-Dimethoxyethyl)-N-methyl-3,4-dimethoxyphenylglycine by Petasis reaction with glyoxylic acid and 3,4-dimethoxyphenylboronic acid.
- Substituted imidazoles via copper-catalyzed reaction with various nitriles.
訊號詞
Warning
危險分類
Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3
標靶器官
Respiratory system
儲存類別代碼
3 - Flammable liquids
水污染物質分類(WGK)
WGK 3
閃點(°F)
84.2 °F
閃點(°C)
29 °C
個人防護裝備
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
其他客户在看
A concise synthesis of tetrahydroisoquinoline-1-carboxylic acids using a Petasis reaction and Pomeranz-Fritsch-Bobbitt cyclization sequence
Tetrahedron, 68(14), 3092-3097 (2012)
Expedient synthesis of substituted imidazoles from nitriles
Tetrahedron Letters, 46(48), 8369-8372 (2005)
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