Cas no 3189-12-6 (1H-Indole,3,5-dimethyl-)
1H-Indole,3,5-dimethyl- structure
Product Name:1H-Indole,3,5-dimethyl-
1H-Indole,3,5-dimethyl- Chemical and Physical Properties
Names and Identifiers
-
- 1H-Indole,3,5-dimethyl-
- 3,5-Dimethyl-indol
- 3,5-dimethylindole
- 3,5-dimethyl-indole
- AC1L40AO
- NSC153659
- SureCN12376
- AKOS006346828
- OFAYMWCMRNLYKN-UHFFFAOYSA-N
- SCHEMBL12376
- NSC 153659
- 1H-Indole, 3,5-dimethyl-
- 3189-12-6
- 98H5IIS5FF
- 3,5-Dimethylindol
- UNII-98H5IIS5FF
- MFCD15523472
- E87010
- DTXSID70185737
- NSC-153659
- 3,5-Dimethyl-1H-indole
- SY342721
-
- Inchi: 1S/C10H11N/c1-7-3-4-10-9(5-7)8(2)6-11-10/h3-6,11H,1-2H3
- InChI Key: OFAYMWCMRNLYKN-UHFFFAOYSA-N
- SMILES: N1C=C(C)C2C=C(C)C=CC1=2
Computed Properties
- Exact Mass: 144.0814
- Monoisotopic Mass: 145.089
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 0
- Heavy Atom Count: 11
- Rotatable Bond Count: 0
- Complexity: 144
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- XLogP3: 3
- Topological Polar Surface Area: 15.8?2
Experimental Properties
- Density: 1.08
- Boiling Point: 278.7°Cat760mmHg
- Flash Point: 118°C
- Refractive Index: 1.635
- PSA: 12.89
- LogP: 2.78470
1H-Indole,3,5-dimethyl- Related Literature
-
Pan He,Yufeng Du,Gang Liu,Changsheng Cao,Yanhui Shi,Juan Zhang,Guangsheng Pang RSC Adv. 2013 3 18345
-
2. N–H Insertion reactions of rhodium carbenoids. Part 3.1 The development of a modified Bischler indole synthesis and a new protecting-group strategy for indolesKatherine E. Bashford,Anthony L. Cooper,Peter D. Kane,Christopher J. Moody,Sendogagounder Muthusamy,Elizabeth Swann J. Chem. Soc. Perkin Trans. 1 2002 1672
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3. NotesR. E. Corbett,M. A. McDowall,E. J. Bowen,J. Sahu,C. A. Bunton,G. Israel,M. M. Mhala,D. L. H. Williams,A. R. Katritzky,A. M. Monro,J. A. T. Beard,Peter Bladon,R. L. Huang,C. E. Dalgliesh,W. Kelly,R. A. Cox,A. J. Swallow,G. P. G. Dick,D. Livingston,H. C. S. Wood,G. S. Harris,D. S. Payne,Max Frankel,Y. Knobler,P. A. Fowell,C. T. Mortimer,E. A. Evans,M. Khalifa,A. A. Abo-Ouf,P. Smith,R. Hull,J. Baddiley,J. G. Buchanan,D. H. Hayes,P. A. Smith,M. L. Burstall,M. S. Gibson,E. W. Abel,E. E. Aynsley,M. L. Hair,B. Ellis,V. Petrow,D. Wedlake,R. M. Acheson,G. A. Taylor,Muriel L. Tomlinson,T. H. Elliott J. Chem. Soc. 1958 3715
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