15375-48-1 ((10H-Phenothiazine,10-propyl-)

CAS号:
15375-48-1
英文名称:
10H-Phenothiazine,10-propyl-
分子式:
C15H15NS
分子量:
241.35130238533

10H-Phenothiazine,10-propyl-(15375-48-1)名称与标识符

名称

中文别名:
10-丙基-10H-吩噻嗪;
英文别名:
10H-Phenothiazine,10-propyl-;10-propylphenothiazine;N-(n-Propyl)-phenothiazine;10-n-Propyl-phenothiazin;10-propyl-10H-phenothiazine;10-Propyl-phenothiazin;10-propyl-phenothiazine;10-Propyl-phenthiazin;5-N-Propylphenothiazin;AC1L5DSO;AC1Q2XWQ;AC1Q7G51;N-propylphenothiazine;NSC14198;NSC49371;SureCN343282;10-Propyl-10H-phenothiazine (ACI);Phenothiazine, 10-propyl- (6CI, 7CI, 8CI);NSC 14198;NSC 49371;15375-48-1;AKOS024338535;F77465;SCHEMBL343282;10H-Phenothiazine, 10-propyl-;DTXSID80279813;NSC-14198;NSC-49371;CHEMBL4797915;

标识符

InChIKey:
LNXZDZDPYBPHAM-UHFFFAOYSA-N
Inchi:
1S/C15H15NS/c1-2-11-16-12-7-3-5-9-14(12)17-15-10-6-4-8-13(15)16/h3-10H,2,11H2,1H3
SMILES:
S1C2C(=CC=CC=2)N(CCC)C2C1=CC=CC=2

10H-Phenothiazine,10-propyl-(15375-48-1)物化性质

实验特性

  • LogP : 4.76430
  • PSA : 3.24
  • 折射率 : 1.629
  • 沸点 : 368.6°C at 760 mmHg
  • 闪点 : 176.7°C
  • 密度 : 1.145

计算特性

  • 精确分子量 : 241.09265
  • 氢键供体数量 : 0
  • 氢键受体数量 : 2
  • 可旋转化学键数量 : 2
  • 同位素质量 : 241.093
  • 重原子数量 : 17
  • 复杂度 : 233
  • 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) : 5
  • 拓扑分子极性表面积 : 28.5Ų

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10H-Phenothiazine,10-propyl-(15375-48-1)合成路线

合成路线:1 步
反应条件:
参考文献:
NIR-Absorbing 1,1,4,4-Tetracyanobuta-1,3-diene- and Dicyanoquinodimethane-Functionalized Donor-Acceptor Phenothiazine Derivatives: Synthesis and Characterization
Gupta, Pankaj Kumar; Khan, Faizal; Misra, Rajneesh, Journal of Organic Chemistry, 2023, 88(20), 14308-14322
合成路线:1 步
反应条件:
参考文献:
Orange to red emissive aldehyde substituted donor-π-acceptor phenothiazine derivatives: optoelectronic, DFT and thermal studies
Mantur, Shivaraj ; Patil, Mallikarjun Kalagouda ; Nadaf, Afra Quasar Abdul Rasheed ; Najare, Mahesh Sadashivappa ; Yaseen, Mohammed ; et al, European Journal of Chemistry, 2023, 14(1), 16-29
合成路线:1 步
反应条件:
参考文献:
Structure-activity relationship studies of phenothiazine derivatives as a new class of ferroptosis inhibitors together with the therapeutic effect in an ischemic stroke model
Yang, Wei; Liu, Xiaolong; Song, Chunli; Ji, Sen; Yang, Jianhong; et al, European Journal of Medicinal Chemistry, 2021, 209, 112842
合成路线:1 步
反应条件:
参考文献:
Synthesis, characterization and photophysical properties of π-conjugated novel phenothiazine substituted acrylonitrile D-A derivatives: Orange to red emission
Mantur, Shivaraj; Patil, Mallikarjun K.; Nadaf, AfraQuasar A.; Najare, Mahesh S.; Yaseen, Mohammed; et al, Chemical Data Collections, 2020, 30, 100543
合成路线:1 步
反应条件:
参考文献:
White hyperelectrofluorescence from solution-processable OLEDs based on phenothiazine substituted tetraphenylethylene derivatives
Khan, Faizal; Urbonas, Ervinas; Volyniuk, Dmytro; Grazulevicius, Juozas V.; Mobin, Shaikh M.; et al, Journal of Materials Chemistry C: Materials for Optical and Electronic Devices, 2020, 8(38), 13375-13388