920979-04-0 (3-氨基-2-碘-6-(三氟甲基)-吡啶,2-Iodo-6-(trifluoromethyl)pyridin-3-amine)

CAS号:
920979-04-0
中文名称:
3-氨基-2-碘-6-(三氟甲基)-吡啶
英文名称:
2-Iodo-6-(trifluoromethyl)pyridin-3-amine
分子式:
C6H4F3IN2
分子量:
288.009043693542

3-氨基-2-碘-6-(三氟甲基)-吡啶(920979-04-0)名称与标识符

名称

中文别名:
2-氟-3-碘-6-甲基吡啶;3-氨基-2-碘-6-(三氟甲基)-吡啶;
英文别名:
2-Iodo-6-(trifluoromethyl)pyridin-3-amine;3-Amino-2-iodo-6-(trifluoromethyl)-pyridine;3-Pyridinamine,2-iodo-6-(trifluoromethyl)-;5-Amino-6-iodo-2-(trifluoromethyl)pyridine;3-amino-2-iodo-6-(trifluoromethyl)pyridine;AK103238;PGLQPMZEWVGHHQ-UHFFFAOYSA-N;FCH1401809;3-amino-2-iodo-6-trifluoromethylpyridine;2-iodo-6-trifluoromethylpyridin-3-ylamine;2-iodo-6-trifluoromethyl-pyridin-3-ylamine;AX8234777;ST24040;2-Iodo-6-(trifluoromethyl)-3-pyridinamine (ACI);(2-Iodo-6-trifluoromethylpyridin-3-yl)amine;J-509719;DS-4051;MFCD11044265;DB-082111;SCHEMBL830696;920979-04-0;AKOS015995179;2-Iodo-6-(trifluoromethyl)pyridin-3-ylamine;SB82353;DTXSID20698887;C77151;

标识符

MDL:
MFCD11044265
InChIKey:
PGLQPMZEWVGHHQ-UHFFFAOYSA-N
Inchi:
1S/C6H4F3IN2/c7-6(8,9)4-2-1-3(11)5(10)12-4/h1-2H,11H2
SMILES:
FC(C1C=CC(N)=C(I)N=1)(F)F

3-氨基-2-碘-6-(三氟甲基)-吡啶(920979-04-0)物化性质

实验特性

  • LogP : 2.86840
  • PSA : 38.91000
  • 折射率 : 1.586
  • 沸点 : 233.1°C at 760 mmHg
  • 闪点 : 94.8°C
  • 密度 : 1.892

计算特性

  • 精确分子量 : 287.93700
  • 氢键供体数量 : 1
  • 氢键受体数量 : 5
  • 可旋转化学键数量 : 0
  • 同位素质量 : 287.937
  • 重原子数量 : 12
  • 复杂度 : 161
  • 同位素原子数量 : 0
  • 确定原子立构中心数量 : 0
  • 不确定原子立构中心数量 : 0
  • 确定化学键立构中心数量 : 0
  • 不确定化学键立构中心数量 : 0
  • 共价键单元数量 : 1
  • 疏水参数计算参考值(XlogP) : 1.8
  • 拓扑分子极性表面积 : 38.9

3-氨基-2-碘-6-(三氟甲基)-吡啶(920979-04-0)推荐厂家 更多厂家(14)

3-氨基-2-碘-6-(三氟甲基)-吡啶(920979-04-0)合成路线

合成路线:1 步
反应条件:
参考文献:
New pyrrolopyridine derivatives and their preparation and use as PPAR activators
, World Intellectual Property Organization, , ,
合成路线:1 步
反应条件:
参考文献:
New pyrrolopyridine compounds, their preparation and use as PPAR activators
, France, , ,
合成路线:1 步
反应条件:
参考文献:
Preparation of 4-phenylpiperidine-substituted amino acid derivatives, particularly valine amides, as modulators of chemokine receptor activity and their use in the treatment of inflammatory and autoimmune diseases
, World Intellectual Property Organization, , ,
合成路线:1 步
反应条件:
参考文献:
Process for preparation of PARP7 inhibitor
, World Intellectual Property Organization, , ,
合成路线:1 步
反应条件:
参考文献:
Isoindolines as HDAC inhibitors and their preparation
, World Intellectual Property Organization, , ,
合成路线:1 步
反应条件:
参考文献:
Preparation of arylsulfonyl-(pyrrolidine or piperidine)-2-carboxamide as TRPA1 antagonists useful in treatment TRPA1-mediated diseases
, World Intellectual Property Organization, , ,
合成路线:1 步
反应条件:
参考文献:
Preparation of N-(thiophen-3-yl)acetamide derivatives as inhibitors of JNK N-terminal kinase
, World Intellectual Property Organization, , ,
合成路线:1 步
反应条件:
参考文献:
Preparation of N-(aminoheteroaryl)-1H-pyrrolopyridine-2-carboxamides as VR1 type capsaicin receptor antagonists
, World Intellectual Property Organization, , ,
合成路线:1 步
反应条件:
参考文献:
Preparation of tricyclic N-(heteroaryl)-carboxamide derivatives as VR1 type capsaicin receptor ligands
, World Intellectual Property Organization, , ,
合成路线:1 步
参考文献:
Preparation of 4-phenylpiperidine-substituted amino acid derivatives, particularly valine amides, as modulators of chemokine receptor activity and their use in the treatment of inflammatory and autoimmune diseases
, United States, , ,
合成路线:1 步
参考文献:
Preparation of N-(aminoheteroaryl)-1H-pyrrolopyridine-2-carboxamides as VR1 type capsaicin receptor antagonists
, France, , ,
合成路线:1 步
参考文献:
Preparation of 1-(arylalkyl)-1H-pyrrolopyridine-2-carboxamide derivatives as VR1 type capsaicin receptor antagonists
, World Intellectual Property Organization, , ,

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