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939-26-4 | 2-(Bromomethyl)Naphthalene
CAS No: 939-26-4 Catalog No: AG0032V6 MDL No:MFCD00004123
Product Description
Catalog Number:
AG0032V6
Chemical Name:
2-(Bromomethyl)Naphthalene
CAS Number:
939-26-4
Molecular Formula:
C11H9Br
Molecular Weight:
221.0932
MDL Number:
MFCD00004123
IUPAC Name:
2-(bromomethyl)naphthalene
InChI:
InChI=1S/C11H9Br/c12-8-9-5-6-10-3-1-2-4-11(10)7-9/h1-7H,8H2
InChI Key:
RUHJZSZTSCSTCC-UHFFFAOYSA-N
SMILES:
BrCc1ccc2c(c1)cccc2
EC Number:
213-359-5
Properties
Complexity:
144
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
219.989g/mol
Formal Charge:
0
Heavy Atom Count:
12
Hydrogen Bond Acceptor Count:
0
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
221.097g/mol
Monoisotopic Mass:
219.989g/mol
Rotatable Bond Count:
1
Topological Polar Surface Area:
0A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
3.7
Literature
| Title | Journal |
|---|---|
| A naphthalene exciplex based Al3+ selective on-type fluorescent probe for living cells at the physiological pH range: experimental and computational studies. | The Analyst 20120507 |
| 1,3-Bis(naphthalen-2-ylmeth-yl)-1H-anthra[1,2-d]imidazole-2,6,11(3H)-trione. | Acta crystallographica. Section E, Structure reports online 20110801 |
| A Cu2+ ion-selective fluoroionophore with dual off/on switches. | Chemistry Central journal 20100101 |
| Distributed Drug Discovery, Part 3: using D(3) methodology to synthesize analogs of an anti-melanoma compound. | Journal of combinatorial chemistry 20090112 |
| Distributed Drug Discovery, Part 2: global rehearsal of alkylating agents for the synthesis of resin-bound unnatural amino acids and virtual D(3) catalog construction. | Journal of combinatorial chemistry 20090112 |
| Anticancer Activity of Ag(I) N-Heterocyclic Carbene Complexes Derived from 4,5-Dichloro-1H-Imidazole. | Metal-based drugs 20080101 |
| Preparation and isolation of dithiolene thiophosphoryl molecules as stable, protected forms of dithiolene ligands. | Inorganic chemistry 20070416 |
| Synthesis and properties of a new member of the calixnaphthalene family: a C(2)-symmetrical endo-calix[4]naphthalene. | The Journal of organic chemistry 20020920 |
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