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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

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

Synthesis, antiprotozoal and antibacterial activity of nitro- and halogeno-substituted benzimidazole derivatives.

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)


More Articles


Related Compounds