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About This Item
Linear Formula:
C10H7CH2Cl
CAS Number:
Molecular Weight:
176.64
EC Number:
201-678-2
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
Beilstein/REAXYS Number:
636885
MDL number:
Assay:
≥97.0% (GC)
Form:
solid
grade
technical
Quality Level
assay
≥97.0% (GC)
form
solid
color
deep brown
refractive index
n20/D 1.635
bp
167-169 °C/25 mmHg (lit.)
mp
32 °C (lit.)
density
1.18 g/mL at 25 °C (lit.)
functional group
chloro
SMILES string
ClCc1cccc2ccccc12
InChI
1S/C11H9Cl/c12-8-10-6-3-5-9-4-1-2-7-11(9)10/h1-7H,8H2
InChI key
XMWGTKZEDLCVIG-UHFFFAOYSA-N
General description
Kinetics and dissociation mechanism of 1-(chloromethyl)naphthalene following 266nm photoexcitation has been studied. Intermolecular nucleophilic dearomatization of 1-chloromethyl naphthalene with various activated methylene compounds has been investigated.
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signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1B
Storage Class
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
269.6 °F - closed cup
flash_point_c
132 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
Regulatory Information
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Bo Peng et al.
Organic letters, 13(19), 5402-5405 (2011-09-14)
Palladium-catalyzed nucleophilic dearomatization of chloromethyl naphthalene derivatives to produce ortho- or para-substituted carbocycles in satisfactory to excellent yields has been developed. The unprecedented dearomatization reactions proceeded smoothly under mild conditions via η(3)-benzylpalladium intermediates.
Formation kinetics and spectra of aromatic radicals in solution.
Kelley DF, et al.
The Journal of Physical Chemistry, 87(11), 1842-1843 (1983)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 25170-50ML | 04061825937908 |

