Home Halogens 1H-Indole,2-chloro-(9CI)

1H-Indole,2-chloro-(9CI)

CAS No.:
7135-31-1
Catalog Number:
AG00FFZK
Molecular Formula:
C8H6ClN
Molecular Weight:
151.5929
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Product Description
Catalog Number:
AG00FFZK
Chemical Name:
1H-Indole,2-chloro-(9CI)
CAS Number:
7135-31-1
Molecular Formula:
C8H6ClN
Molecular Weight:
151.5929
MDL Number:
MFCD04117990
IUPAC Name:
2-chloro-1H-indole
InChI:
InChI=1S/C8H6ClN/c9-8-5-6-3-1-2-4-7(6)10-8/h1-5,10H
InChI Key:
HBZHNVUMFPGVHW-UHFFFAOYSA-N
SMILES:
Clc1cc2c([nH]1)cccc2
Properties
Complexity:
126  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
151.019g/mol
Formal Charge:
0
Heavy Atom Count:
10  
Hydrogen Bond Acceptor Count:
0
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0
Molecular Weight:
151.593g/mol
Monoisotopic Mass:
151.019g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
15.8A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
3.4  
Literature
Title Journal
Peculiarity of methoxy group-substituted phenylhydrazones in Fischer indole synthesis. Proceedings of the Japan Academy. Series B, Physical and biological sciences 20120111
Enabling large-scale design, synthesis and validation of small molecule protein-protein antagonists. PloS one 20120101
Specific sequence motifs direct the oxygenation and chlorination of tryptophan by myeloperoxidase. Biochemistry 20060328
Substituted E-3-(2-Chloro-3-indolylmethylene)1,3-dihydroindol-2-ones with antitumor activity. Bioorganic & medicinal chemistry 20040301
Carbonic anhydrase inhibitors: E7070, a sulfonamide anticancer agent, potently inhibits cytosolic isozymes I and II, and transmembrane, tumor-associated isozyme IX. Bioorganic & medicinal chemistry letters 20040105
Synthesis and antitumor activity of 1,5,6-substituted E-3-(2-chloro-3-indolylmethylene)-1,3-dihydroindol-2-ones. Journal of medicinal chemistry 20020606
Properties