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Home > Imidazoles > 3652-92-4
3652-92-4 | 1,3-Dimethyl-1,3-dihydro-2-phenyl-2H-benzimidazole
CAS No: 3652-92-4 Catalog No: AG00CKE5 MDL No:
Product Description
Catalog Number:
AG00CKE5
Chemical Name:
1,3-Dimethyl-1,3-dihydro-2-phenyl-2H-benzimidazole
CAS Number:
3652-92-4
IUPAC Name:
1,3-dimethyl-2-phenyl-2H-benzimidazole
InChI:
InChI=1S/C15H16N2/c1-16-13-10-6-7-11-14(13)17(2)15(16)12-8-4-3-5-9-12/h3-11,15H,1-2H3
InChI Key:
VDFIVJSRRJXMAU-UHFFFAOYSA-N
Properties
Complexity:
242
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
224.131g/mol
Formal Charge:
0
Heavy Atom Count:
17
Hydrogen Bond Acceptor Count:
2
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
224.307g/mol
Monoisotopic Mass:
224.131g/mol
Rotatable Bond Count:
1
Topological Polar Surface Area:
6.5A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
3.6
Literature
| Title | Journal |
|---|---|
| Synthesis and SAR studies of 1,4-benzoxazine MenB inhibitors: novel antibacterial agents against Mycobacterium tuberculosis. | Bioorganic & medicinal chemistry letters 20101101 |
| Primary kinetic isotope effects on hydride transfer from heterocyclic compounds to NAD(+) analogues. | The journal of physical chemistry. A 20091008 |
| Photosonochemical catalytic ring opening of alpha-epoxyketones. | Beilstein journal of organic chemistry 20070101 |
| Contrastive photoreduction pathways of benzophenones governed by regiospecific deprotonation of imidazoline radical cations and additive effects. | The Journal of organic chemistry 20051111 |
| Primary kinetic isotope effects on hydride transfer from 1,3-dimethyl-2-phenylbenzimidazoline to NAD(+) analogues. | Journal of the American Chemical Society 20010808 |
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