反应 #4148334
相关文献 (1)
openreactiondata ↗doi:10.1039/C8SC04228D
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-e3415053406041148a19ec5b0da07b27暂无可渲染的结构数据
CCNC(=O)Cl产品信息
Carbamic chloride, ethyl-(CAS 41891-13-8)的产品身份、结构标识及相关反应资料,供化学中间体检索、研发和采购评估使用。
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12 条反应 · 12 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-e3415053406041148a19ec5b0da07b27反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-e3415053406041148a19ec5b0da07b27反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: When diethylcarbamylchloride is replaced in the above procedure by carbamyl chloride (prepared in situ from potassium cyanate and anhydrous hydrogen chloride in anhydrous chloroform), ethylcarbamyl chloride or dimethylcarbamyl chloride, then the products prepared are α-carbamylthio2'-chloro-4-biphenylylacetic acid, α-ethylcarbamylthio-2'-chloro-4-biphenylylacetic acid or α-dimethylcarbamylthio-2'-chloro-4-biphenylylacetic acid. the products prepared
来源 ID: ord-92812363b4e14ecfb4da9e08a1558a01反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: When diethylcarbamylchloride is replaced in the above procedure by carbamyl chloride (prepared in situ from potassium cyanate and anhydrous hydrogen chloride in anhydrous chloroform), ethylcarbamyl chloride or dimethylcarbamyl chloride, then the products prepared are α-carbamylthio2'-chloro-4-biphenylylacetic acid, α-ethylcarbamylthio-2'-chloro-4-biphenylylacetic acid or α-dimethylcarbamylthio-2'-chloro-4-biphenylylacetic acid. the products prepared
来源 ID: ord-92812363b4e14ecfb4da9e08a1558a01反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Employing the same procedure as described in Example 4, diethylcarbamyl chloride, diphenylcarbamyl chloride, ethylcarbamyl chloride and N-methyl, N-phenyl carbamyl chloride were respectively reacted with 1-hydroxyanthraquinone in pyridine to obtain the corresponding 1-anthraquinonyl carbamate derivatives.
来源 ID: ord-0ace4a359ecf44dcbe95a408d7a7094d反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Employing the same procedure as described in Example 4, diethylcarbamyl chloride, diphenylcarbamyl chloride, ethylcarbamyl chloride and N-methyl, N-phenyl carbamyl chloride were respectively reacted with 1-hydroxyanthraquinone in pyridine to obtain the corresponding 1-anthraquinonyl carbamate derivatives.
来源 ID: ord-0ace4a359ecf44dcbe95a408d7a7094d反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: When diethylcarbamylchloride is replaced in the above procedure by carbamyl chloride (prepared in situ from potassium cyanate and anhydrous hydrogen chloride in anhydrous chloroform), ethylcarbamyl chloride or dimethylcarbamyl chloride, then the products prepared are α-carbamylthio2'-chloro-4-biphenylylacetic acid, α-ethylcarbamylthio-2'-chloro-4-biphenylylacetic acid or α-dimethylcarbamylthio-2'-chloro-4-biphenylylacetic acid. the products prepared
来源 ID: ord-92812363b4e14ecfb4da9e08a1558a01反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: When diethylcarbamylchloride is replaced in the above procedure by carbamyl chloride (prepared in situ from potassium cyanate and anhydrous hydrogen chloride in anhydrous chloroform), ethylcarbamyl chloride or dimethylcarbamyl chloride, then the products prepared are α-carbamylthio2'-chloro-4-biphenylylacetic acid, α-ethylcarbamylthio-2'-chloro-4-biphenylylacetic acid or α-dimethylcarbamylthio-2'-chloro-4-biphenylylacetic acid. the products prepared
来源 ID: ord-92812363b4e14ecfb4da9e08a1558a01反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: When diethylcarbamylchloride is replaced in the above procedure by carbamyl chloride (prepared in situ from potassium cyanate and anhydrous hydrogen chloride in anhydrous chloroform), ethylcarbamyl chloride or dimethylcarbamyl chloride, then the products prepared are α-carbamylthio-6-methoxy-2-naphthylacetic acid, α-ethylcarbamylthio-6-methoxy-2-naphthylacetic acid or α-dimethylcarbamylthio-6-methoxy-2-naphthylacetic acid. the products prepared
来源 ID: ord-223595e68bfe40c3bf6bc68e0ad04983反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: When diethylcarbamylchloride is replaced in the above procedure by carbamyl chloride (prepared in situ from potassium cyanate and anhydrous hydrogen chloride in anhydrous chloroform), ethylcarbamyl chloride or dimethylcarbamyl chloride, then the products prepared are α-carbamylthio-3-chloro-4-cyclohexylphenylacetic acid, α-ethylcarbamylthio-3-chloro-4-cyclohexylphenylacetic acid or α-dimethylcarbamylthio-3-chloro-4-cyclohexylphenylacetic acid. the products prepared
来源 ID: ord-92c1e3e7e8c844cd84ce9c0ca68eed92反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Employing the same procedure as described in Example 4, diethylcarbamyl chloride, diphenylcarbamyl chloride, ethylcarbamyl chloride and N-methyl, N-phenyl carbamyl chloride were respectively reacted with 1-hydroxyanthraquinone in pyridine to obtain the corresponding 1-anthraquinonyl carbamate derivatives.
来源 ID: ord-0ace4a359ecf44dcbe95a408d7a7094d反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: When diethylcarbamylchloride is replaced in the above procedure by carbamyl chloride (prepared in situ from potassium cyanate and anhydrous hydrogen chloride in anhydrous chloroform), ethylcarbamyl chloride or dimethylcarbamyl chloride, then the products prepared are α-carbamylthio2'-chloro-4-biphenylylacetic acid, α-ethylcarbamylthio-2'-chloro-4-biphenylylacetic acid or α-dimethylcarbamylthio-2'-chloro-4-biphenylylacetic acid. the products prepared
来源 ID: ord-92812363b4e14ecfb4da9e08a1558a01PubChem References
以下资料来自该化合物的公开数据库参考记录。
