799293-73-5 (3 - 溴呋喃并[3,2-C]吡啶-4 - 胺,3-Bromofuro[3,2-c]pyridin-4-amine)

CAS号:
799293-73-5
中文名称:
3 - 溴呋喃并[3,2-C]吡啶-4 - 胺
英文名称:
3-Bromofuro[3,2-c]pyridin-4-amine
分子式:
C7H5BrN2O
分子量:
213.031400442123

3 - 溴呋喃并[3,2-C]吡啶-4 - 胺(799293-73-5)名称与标识符

名称

中文别名:
3 - 溴呋喃并[3,2-C]吡啶-4 - 胺;
英文别名:
3-Bromofuro[3,2-c]pyridin-4-amine;3-bromo-Furo[3,2-c]pyridin-4-amine;Furo[3,2-c]pyridin-4-amine, 3-bromo-;OAWQPZKVGXRJSX-UHFFFAOYSA-N;2485AC;FCH1365118;Furo[3,2-c]pyridin-4-amine,3-bromo-;3-bromo-furo[3,2-c]pyridin-4-ylamine;4-Amino-3-bromo-furo[3,2-c]pyridine;EN000030;AX8237832;3-Bromofuro[3,2-c]pyridin-4-amine (ACI);DTXSID50593952;DS-16075;SCHEMBL758987;799293-73-5;AKOS016007046;FT-0704875;ZGB29373;MFCD18254917;DA-23926;

标识符

MDL:
MFCD18254917
InChIKey:
OAWQPZKVGXRJSX-UHFFFAOYSA-N
Inchi:
1S/C7H5BrN2O/c8-4-3-11-5-1-2-10-7(9)6(4)5/h1-3H,(H2,9,10)
SMILES:
BrC1C2C(=CC=NC=2N)OC=1

3 - 溴呋喃并[3,2-C]吡啶-4 - 胺(799293-73-5)物化性质

实验特性

  • LogP : 2.10260
  • PSA : 52.78000
  • 沸点 : 346.7±37.0℃ at 760 mmHg

计算特性

  • 精确分子量 : 211.95900
  • 氢键供体数量 : 1
  • 氢键受体数量 : 3
  • 可旋转化学键数量 : 0
  • 同位素质量 : 211.95853g/mol
  • 重原子数量 : 11
  • 复杂度 : 155
  • 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) : 1.6
  • 拓扑分子极性表面积 : 52

3 - 溴呋喃并[3,2-C]吡啶-4 - 胺(799293-73-5)海关数据

海关编码:
2934999090
海关数据:

中国海关编码:

2934999090

概述:

2934999090. 其他杂环化合物. 增值税率:17.0%. 退税率:13.0%. 监管条件:无. 最惠国关税:6.5%. 普通关税:20.0%

申报要素:

品名, 成分含量, 用途

Summary:

2934999090. other heterocyclic compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

3 - 溴呋喃并[3,2-C]吡啶-4 - 胺(799293-73-5)推荐厂家 更多厂家(10)

3 - 溴呋喃并[3,2-C]吡啶-4 - 胺(799293-73-5)合成路线

合成路线:1 步
反应条件:
参考文献:
Discovery of a New Series of Naphthamides as Potent VEGFR-2 Kinase Inhibitors
Lv, Yongcong; et al, ACS Medicinal Chemistry Letters, 2014, 5(5), 592-597
合成路线:2 步
反应条件:
参考文献:
Design and effective synthesis of novel templates, 3,7-diphenyl-4-amino-thieno and furo-[3,2-c]pyridines as protein kinase inhibitors and in vitro evaluation targeting angiogenetic kinases
Miyazaki, Yasushi; et al, Bioorganic & Medicinal Chemistry Letters, 2007, 17(1), 250-254
合成路线:3 步
反应条件:
参考文献:
Design and effective synthesis of novel templates, 3,7-diphenyl-4-amino-thieno and furo-[3,2-c]pyridines as protein kinase inhibitors and in vitro evaluation targeting angiogenetic kinases
Miyazaki, Yasushi; et al, Bioorganic & Medicinal Chemistry Letters, 2007, 17(1), 250-254
合成路线:4 步
反应条件:
参考文献:
Design and effective synthesis of novel templates, 3,7-diphenyl-4-amino-thieno and furo-[3,2-c]pyridines as protein kinase inhibitors and in vitro evaluation targeting angiogenetic kinases
Miyazaki, Yasushi; et al, Bioorganic & Medicinal Chemistry Letters, 2007, 17(1), 250-254
合成路线:5 步
反应条件:
参考文献:
Design and effective synthesis of novel templates, 3,7-diphenyl-4-amino-thieno and furo-[3,2-c]pyridines as protein kinase inhibitors and in vitro evaluation targeting angiogenetic kinases
Miyazaki, Yasushi; et al, Bioorganic & Medicinal Chemistry Letters, 2007, 17(1), 250-254
合成路线:6 步
反应条件:
参考文献:
Design and effective synthesis of novel templates, 3,7-diphenyl-4-amino-thieno and furo-[3,2-c]pyridines as protein kinase inhibitors and in vitro evaluation targeting angiogenetic kinases
Miyazaki, Yasushi; et al, Bioorganic & Medicinal Chemistry Letters, 2007, 17(1), 250-254