5388-42-1 (2,3-二氢-2-苯基-1H-异吲哚-1-氧代异吲哚啉,2-phenyl-2,3-dihydro-1H-isoindol-1-one)

CAS号:
5388-42-1
中文名称:
2,3-二氢-2-苯基-1H-异吲哚-1-氧代异吲哚啉
英文名称:
2-phenyl-2,3-dihydro-1H-isoindol-1-one
分子式:
C14H11NO
分子量:
209.243243455887

2,3-二氢-2-苯基-1H-异吲哚-1-氧代异吲哚啉(5388-42-1)名称与标识符

名称

中文别名:
2,3-二氢-2-苯基-1H-异吲哚-1-酮;2,3-二氢-2-苯基-1H-异吲哚-1-氧代异吲哚啉;
英文别名:
1H-Isoindol-1-one,2,3-dihydro-2-phenyl-;2,3-DIHYDRO-2-PHENYL-1H-ISOINDOL-1-OXO-ISOINDOLINE;Phthalimidine, 2-phenyl-;2,3-dihydro-2-phenyl-1h-isoindol-1-on;2,3-Dihydro-2-phenyl-1H-isoindol-1-one;2-phenyl-2,3-dihydro-isoindol-1-one;2-Phenyl-2H-isoindol-1(3H)-one;2-phenyl-3H-isoindol-1-one;2-Phenylisoindolin-1-one;2-phenyl-phthalimidin;4-N-phenylisoindolinone;N-phenyl-1-isoindo;N-Phenyl-1-isoindolinone;N-phenylisoindolin-1-one;N-phenylisoindoline-1-one;N-phenylisoindolone;n-phenylphthalimidine;PHTHALIMIDE,2-PHENYL-;2-Phenyl-1-oxoisoindoline;2-phenyl-2,3-dihydro-1H-isoindol-1-one;U8M4WOJ0XS;1H-Isoindol-1-one, 2,3-dihydro-2-phenyl-;FIWLYGQHSKZFAQ-UHFFFAOYSA-N;1H-Isoindol-1-one, 2,3-dihydro-2-phenyl- (9CI);phenylisoindolinone;NSC97577;2-Phenyl-1-isoindolinone;2-Phenyl-1-isoindolinone #;MLS001204877;SMR000514256;SB66119;SR-01000359852-1;F1172-0012;NS-02319;BRN 0149773;NSC 97577;DTXSID10202134;5388-42-1;CHEMBL1568952;NSC-97577;1H-Isoindol-1-one,3-dihydro-2-phenyl-;AKOS000523431;UNII-U8M4WOJ0XS;NCGC00245136-01;SCHEMBL4188221;CCG-274907;AE-848/32184055;HMS1677E05;MFCD00023020;BRD-K29397763-001-10-8;CS-0156109;SR-01000359852;HMS2813G18;5-21-08-00020 (Beilstein Handbook Reference);STL119777;BBL018973;

标识符

MDL:
MFCD00023020
InChIKey:
FIWLYGQHSKZFAQ-UHFFFAOYSA-N
Inchi:
1S/C14H11NO/c16-14-13-9-5-4-6-11(13)10-15(14)12-7-2-1-3-8-12/h1-9H,10H2
SMILES:
O=C1C2C=CC=CC=2CN1C1C=CC=CC=1
BRN:
0149773

2,3-二氢-2-苯基-1H-异吲哚-1-氧代异吲哚啉(5388-42-1)物化性质

实验特性

  • PSA : 20.31
  • 折射率 : 1.5780 (estimate)
  • 沸点 : 348.61°C (rough estimate)
  • 熔点 : 162.5°C
  • 闪点 : 180.8°C
  • 密度 : 1.0966 (rough estimate)

计算特性

  • 精确分子量 : 209.08413
  • 氢键供体数量 : 0
  • 氢键受体数量 : 1
  • 可旋转化学键数量 : 1
  • 同位素质量 : 209.084
  • 重原子数量 : 16
  • 复杂度 : 270
  • 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) : 2.7
  • 拓扑分子极性表面积 : 20.3

2,3-二氢-2-苯基-1H-异吲哚-1-氧代异吲哚啉(5388-42-1)国际标准相关数据

EINECS:
97577

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2,3-二氢-2-苯基-1H-异吲哚-1-氧代异吲哚啉(5388-42-1)相关文献

  • 1. Application of organolithium and related reagents in synthesis. Part 21.1 Synthetic strategies based on ortho-aromatic metallation. A concise regiospecific synthesis of arylnaphthalanes as precursors of naphthylisoquinoline alkaloids
    Jan Epsztajn,Andrzej Jó?wiak,Aleksandra K. Szcze?niak J. Chem. Soc. Perkin Trans. 1 1998 2563
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  • 3. CXXXVIII.—A new reaction of certain diazosulphonates derived from β-naphthol-l-sulphonic acid. Part VI. Preparation of phthalazine, phthalazone, and phthalimidine derivatives from 2 : 6-dichloro- and 2 : 6-dibromo-4-nitroaniline
    Frederick Maurice Rowe,Charles Dunbar,Norman Henry Williams J. Chem. Soc. 1931 1073
  • 4. CCCXXXVIII.—A new reaction of certain diazosulphonates derived from β-naphthol-1-sulphonic acid. Part III. Preparation of phthalazine, phthalazone, and phthalimidine derivatives from m-nitroaniline
    Frederick Maurice Rowe,Mahmed Ahmed Himmat,Esther Levin J. Chem. Soc. 1928 2556
  • 5. XCVI.—A new reaction of certain diazosulphonates derived from β-naphthol-1-sulphonic acid. Part I. Preparation of phthalazine, phthalazone, and phthalimidine derivatives from 4′-nitrobenzene-2-naphthol-1-diazosulphonate
    Frederick Maurice Rowe,Esther Levin,Alan Chamley Burns,John Stanley Herbert Davies,Wolfe Tepper J. Chem. Soc. 1926 129 690
  • 6. CCCXXXVII.—A new reaction of certain sulphonates derived from β-naphthol-1-sulphoinc acid. Part II. The constitution of nitro- and amino-phenylphthalazones
    Frederick Maurice Rowe,Esther Levin J. Chem. Soc. 1928 2550
  • 7. Formula index
    J. Chem. Soc. 1931 3445
  • 8. Iron carbonyl complexes from Schiff bases
    M. M. Bagga,W. T. Flannigan,G. R. Knox,P. L. Pauson,F. J. Preston,R. I. Reed J. Chem. Soc. C 1968 36
  • 9. Formula index
    J. Chem. Soc. 1928 3370
  • 10. 267. A reaction of certain diazosulphonates derived from β-naphthol-1-sulphonic acid. Part XII. Preparation of phthalazine, phthalazone, and phthalimidine derivatives from 2-bromo-4-nitroaniline
    F. M. Rowe,G. B. Jambuserwala,H. W. Partridge J. Chem. Soc. 1935 1134