3,4-Dichlorobenzyl chloride
Names
[ CAS No. ]:
102-47-6
[ Name ]:
3,4-Dichlorobenzyl chloride
[Synonym ]:
1,2-Dichloro-4-chloromethyl-benzene
1,2-Dichloro-4-(chloromethyl)benzene
Toluene, α,3,4-trichloro-
EINECS 203-033-0
3,4-dichlorophenylmethyl chloride
3,4-Dichlorobenzyl chloride
Benzene, 1,2-dichloro-4-(chloromethyl)-
α,3,4-Trichlorotoluene
MFCD00000906
Chemical & Physical Properties
[ Density]:
1.4±0.1 g/cm3
[ Boiling Point ]:
241.0±0.0 °C at 760 mmHg
[ Melting Point ]:
-3 °C
[ Molecular Formula ]:
C7H5Cl3
[ Molecular Weight ]:
195.474
[ Flash Point ]:
160.2±18.8 °C
[ Exact Mass ]:
193.945679
[ LogP ]:
3.55
[ Vapour Pressure ]:
0.1±0.4 mmHg at 25°C
[ Index of Refraction ]:
1.563
MSDS
Safety Information
[ Symbol ]:
GHS05, GHS07
[ Signal Word ]:
Danger
[ Hazard Statements ]:
H314-H335
[ Precautionary Statements ]:
P261-P280-P305 + P351 + P338-P310
[ Personal Protective Equipment ]:
Faceshields;full-face respirator (US);Gloves;Goggles;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter
[ Hazard Codes ]:
C:Corrosive;
[ Risk Phrases ]:
R34
[ Safety Phrases ]:
S26-S36/37/39-S45
[ RIDADR ]:
UN 3265 8/PG 2
[ WGK Germany ]:
3
[ Packaging Group ]:
III
[ Hazard Class ]:
8
[ HS Code ]:
29036990
Synthetic Route
Precursor & DownStream
Precursor
DownStream
Customs
[ HS Code ]: 2903999090
[ Summary ]:
2903999090 halogenated derivatives of aromatic hydrocarbons VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:5.5% General tariff:30.0%
Articles
Acta Biochim. Pol. 49(1) , 185-95, (2002)
Two series of benzimidazole derivatives were sythesised. The first one was based on 5,6-dinitrobenzimidazole, the second one comprises 2-thioalkyl- and thioaryl-substituted modified benzimidazoles. An...
Friedel-Crafts synthesis of 4-(3, 4-dichlorophenyl)-3, 4-dihydro-1 (2H)-naphthalenone, a key intermediate in the preparation of the antidepressant sertraline. Quallich GJ, et al.J. Org. Chem. 55(16) , 4971-73, (1990)
Syntheses of branched poly (ether ketone) s with pendant functional groups based on 1, 1, 1-tris (4-hydroxyphenyl) ethane. Fritsch D, et al.
J. Macromol. Sci., Part A: Pure Appl. Chem. 39(11) , 1335-47, (2002)