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169255-48-5 | Phenol, 4-iodo-2,6-bis(1-methylethyl)-
CAS No: 169255-48-5 Catalog No: AG00HZA7 MDL No:
Product Description
Catalog Number:
AG00HZA7
Chemical Name:
Phenol, 4-iodo-2,6-bis(1-methylethyl)-
CAS Number:
169255-48-5
IUPAC Name:
4-iodo-2,6-di(propan-2-yl)phenol
InChI:
InChI=1S/C12H17IO/c1-7(2)10-5-9(13)6-11(8(3)4)12(10)14/h5-8,14H,1-4H3
InChI Key:
JMJHJCFWTNRPEI-UHFFFAOYSA-N
Properties
Complexity:
161
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
304.032g/mol
Formal Charge:
0
Heavy Atom Count:
14
Hydrogen Bond Acceptor Count:
1
Hydrogen Bond Donor Count:
1
Isotope Atom Count:
0
Molecular Weight:
304.171g/mol
Monoisotopic Mass:
304.032g/mol
Rotatable Bond Count:
2
Topological Polar Surface Area:
20.2A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
4.5
Literature
| Title | Journal |
|---|---|
| Novel triiodophenol derivatives induce caspase-independent mitochondrial cell death in leukemia cells inhibited by Myc. | Molecular cancer therapeutics 20060501 |
| 4D-QSAR analysis of a set of propofol analogues: mapping binding sites for an anesthetic phenol on the GABA(A) receptor. | Journal of medicinal chemistry 20020718 |
| Anesthetic properties of 4-iodopropofol: implications for mechanisms of anesthesia. | Anesthesiology 20010601 |
| Propofol analogues. Synthesis, relationships between structure and affinity at GABAA receptor in rat brain, and differential electrophysiological profile at recombinant human GABAA receptors. | Journal of medicinal chemistry 19980521 |
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