dinitroacetaldehyde (1,2,4-triazol-3-yl)imine potassium salt
英文别名
——
CAS
138555-30-3
化学式
C4H3N6O4*K
mdl
——
分子量
238.204
InChiKey
ACHXPYVGOQTDOS-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
物化性质
计算性质
ADMET
安全信息
SDS
制备方法与用途
上下游信息
反应信息
文献信息
表征谱图
同类化合物
相关功能分类
相关结构分类
计算性质
辛醇/水分配系数(LogP):
-3.45
重原子数:
15.0
可旋转键数:
4.0
环数:
1.0
sp3杂化的碳原子比例:
0.0
拓扑面积:
140.21
氢给体数:
1.0
氢受体数:
7.0
反应信息
作为产物:
描述:
3-氨基-1,2,4-三氮唑 、 1-anilino-2,2-dinitroethylene potassium salt 以
N,N-二甲基甲酰胺 为溶剂,
反应 5.0h,
以52%的产率得到dinitroacetaldehyde (1,2,4-triazol-3-yl)imine potassium salt
参考文献:
名称:
gem-Dinitro compounds in organic synthesis. 1. Synthesis of functionally substituted polynitro compounds with the use of the universal synthon, ethyl dinitroacetate
摘要:
Ethyl nitroacetate (I) was used as a synthon in the preparation of dinitromethane, dinitroacetic acid, 2,2-dinitroethanol, fluorodinitromethane, 1,1,3,3-tetranitropropane, and some condensation products of Henry and Mannich reactions. A number of dinitroacetaldehyde derivatives were also prepared: its potassium salt, oxime, and hydrazone, dinitroacetaldehyde azine; and mixed azines with other acetaldehydes.