Product Name

  • Name

    1,2-Dichloro-4-(chloromethyl)benzene

  • EINECS 203-033-0
  • CAS No. 102-47-6
  • Article Data11
  • CAS DataBase
  • Density 1.386 g/cm3
  • Solubility
  • Melting Point -3 °C
  • Formula C7H5Cl3
  • Boiling Point 241 °C at 760 mmHg
  • Molecular Weight 195.476
  • Flash Point 160.2 °C
  • Transport Information UN 3265 8/PG 2
  • Appearance Clear to yellowish liquid
  • Safety 26-36/37/39-45
  • Risk Codes 34-36/37
  • Molecular Structure Molecular Structure of 102-47-6 (1,2-Dichloro-4-(chloromethyl)benzene)
  • Hazard Symbols CorrosiveC
  • Synonyms Toluene,a,3,4-trichloro- (7CI,8CI);1,2-Dichloro-4-(chloromethyl)benzene;3,4,a-Trichlorotoluene;3,4-Dichloro-1-(chloromethyl)benzene;3,4-Dichlorophenylmethyl chloride;4-Chloromethyl-1,2-dichlorobenzene;NSC 406893;a,3,4-Trichlorotoluene;
  • PSA 0.00000
  • LogP 3.73220

Synthetic route

3,4-Dichlorotoluene
95-75-0

3,4-Dichlorotoluene

3,4-Dichlorophenylmethyl chloride
102-47-6

3,4-Dichlorophenylmethyl chloride

Conditions
ConditionsYield
With sulfuryl dichloride; dibenzoyl peroxide
With chlorine
With chlorine
benzyl chloride
100-44-7

benzyl chloride

3,4-Dichlorophenylmethyl chloride
102-47-6

3,4-Dichlorophenylmethyl chloride

Conditions
ConditionsYield
With iodine beim Chlorieren;
formaldehyd
50-00-0

formaldehyd

1,2-dichloro-benzene
95-50-1

1,2-dichloro-benzene

3,4-Dichlorophenylmethyl chloride
102-47-6

3,4-Dichlorophenylmethyl chloride

Conditions
ConditionsYield
With hydrogenchloride; zinc(II) chloride
chloromethyl methyl ether
107-30-2

chloromethyl methyl ether

1,2-dichloro-benzene
95-50-1

1,2-dichloro-benzene

3,4-Dichlorophenylmethyl chloride
102-47-6

3,4-Dichlorophenylmethyl chloride

Conditions
ConditionsYield
With sulfuric acid
3,4-dichlorobenzyl alcohol
1805-32-9

3,4-dichlorobenzyl alcohol

3,4-Dichlorophenylmethyl chloride
102-47-6

3,4-Dichlorophenylmethyl chloride

Conditions
ConditionsYield
With thionyl chloride In toluene for 0.0833333h; Ambient temperature;
With thionyl chloride In dichloromethane at 0 - 20℃; for 3h;
With thionyl chloride at 60℃; for 2h;
3,4-dichlorobenzaldehyde
6287-38-3

3,4-dichlorobenzaldehyde

3,4-Dichlorophenylmethyl chloride
102-47-6

3,4-Dichlorophenylmethyl chloride

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: NaBH4 / methanol / Ambient temperature
2: SOCl2 / toluene / 0.08 h / Ambient temperature
View Scheme
Multi-step reaction with 2 steps
1: sodium tetrahydroborate; methanol / 1 h / 0 - 20 °C
2: thionyl chloride / dichloromethane / 3 h / 0 - 20 °C
View Scheme
3,4-dichlorbenzoic acid
51-44-5

3,4-dichlorbenzoic acid

3,4-Dichlorophenylmethyl chloride
102-47-6

3,4-Dichlorophenylmethyl chloride

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: borane-THF / tetrahydrofuran / 2 h / 0 - 20 °C
2: thionyl chloride / 2 h / 60 °C
View Scheme
3,4-Dichlorophenylmethyl chloride
102-47-6

3,4-Dichlorophenylmethyl chloride

1-(azidomethyl)-3,4-dichlorobenzene
99613-63-5

1-(azidomethyl)-3,4-dichlorobenzene

Conditions
ConditionsYield
With sodium azide In dimethyl sulfoxide at 20℃;100%
With sodium azide In dimethyl sulfoxide at 20℃;100%
With sodium azide In dimethyl sulfoxide at 20℃; Product distribution / selectivity;100%
O7-demethyl glaziovianin A
1252801-64-1

O7-demethyl glaziovianin A

3,4-Dichlorophenylmethyl chloride
102-47-6

3,4-Dichlorophenylmethyl chloride

7-((3,4-dichlorobenzyl)oxy)-3-(4,7-dimethoxybenzo[d][1,3]dioxol-5-yl)-6-methoxy-4H-chromen-4-one

7-((3,4-dichlorobenzyl)oxy)-3-(4,7-dimethoxybenzo[d][1,3]dioxol-5-yl)-6-methoxy-4H-chromen-4-one

Conditions
ConditionsYield
With potassium carbonate In acetonitrile for 18h; Reflux;100%
3,4-Dichlorophenylmethyl chloride
102-47-6

3,4-Dichlorophenylmethyl chloride

2,2'-iminobis[ethanol]
111-42-2

2,2'-iminobis[ethanol]

2-[(2-Hydroxy-ethyl)-(3,4-dichloro-benzyl)-amino]-ethanol
60876-94-0

2-[(2-Hydroxy-ethyl)-(3,4-dichloro-benzyl)-amino]-ethanol

Conditions
ConditionsYield
With potassium carbonate In acetone for 8h; Heating;99%
99%
99%
3,4-Dichlorophenylmethyl chloride
102-47-6

3,4-Dichlorophenylmethyl chloride

6-methanesulphonyl-2(3H)-benzoxazolone
43115-48-6

6-methanesulphonyl-2(3H)-benzoxazolone

3-(3,4-dichlorobenzyl)-6-methanesulphonyl-2(3H)-benzoxazolone
483288-06-8

3-(3,4-dichlorobenzyl)-6-methanesulphonyl-2(3H)-benzoxazolone

Conditions
ConditionsYield
Stage #1: 6-methanesulphonyl-2(3H)-benzoxazolone With potassium carbonate In N,N-dimethyl-formamide at 70℃; for 1h;
Stage #2: 3,4-Dichlorophenylmethyl chloride In N,N-dimethyl-formamide at 70℃; for 2h;
98%
indole-2,3-dione
91-56-5

indole-2,3-dione

3,4-Dichlorophenylmethyl chloride
102-47-6

3,4-Dichlorophenylmethyl chloride

1-(3,4-Dichlorobenzyl)-1H-indole-2,3-dione

1-(3,4-Dichlorobenzyl)-1H-indole-2,3-dione

Conditions
ConditionsYield
With caesium carbonate In N,N-dimethyl-formamide at 20℃; for 24h;98%
3,4-Dichlorophenylmethyl chloride
102-47-6

3,4-Dichlorophenylmethyl chloride

3-mercapto-1,2,4-triazole
3179-31-5

3-mercapto-1,2,4-triazole

3-(3,4-dichloro-benzylsulfanyl)-4H-[1,2,4]triazole

3-(3,4-dichloro-benzylsulfanyl)-4H-[1,2,4]triazole

Conditions
ConditionsYield
Stage #1: 3-mercapto-1,2,4-triazole With sodium In methanol; 1,2-dimethoxyethane at 20℃; for 0.166667h;
Stage #2: 3,4-Dichlorophenylmethyl chloride In methanol; 1,2-dimethoxyethane at 20℃; for 4h;
97%
N'-[5-chloro-2-(1-naphthylthio)phenyl]-N,N-dimethylpropan-1,3-diamine
1100795-02-5

N'-[5-chloro-2-(1-naphthylthio)phenyl]-N,N-dimethylpropan-1,3-diamine

3,4-Dichlorophenylmethyl chloride
102-47-6

3,4-Dichlorophenylmethyl chloride

3-({5-chloro-2-[1-naphthylthio]phenyl}amino)-N-(3,4-dichlorobenzyl)-N,N-dimethylpropan-1-ammonium chloride
1100795-11-6

3-({5-chloro-2-[1-naphthylthio]phenyl}amino)-N-(3,4-dichlorobenzyl)-N,N-dimethylpropan-1-ammonium chloride

Conditions
ConditionsYield
In acetone at 120℃; for 0.333333h; Inert atmosphere; Microwave irradiation;97%
2-bromo-4-chlorophenol
695-96-5

2-bromo-4-chlorophenol

3,4-Dichlorophenylmethyl chloride
102-47-6

3,4-Dichlorophenylmethyl chloride

1-bromo-5-chloro-2-(3,4-dichlorobenzyloxy)benzene

1-bromo-5-chloro-2-(3,4-dichlorobenzyloxy)benzene

Conditions
ConditionsYield
With potassium carbonate; potassium iodide In acetone at 60℃; for 24h; Inert atmosphere;95%
1-(2-benzoyl-4-chlorophenyl)-3-[(2S)-2-methylpyrrolidine-2-carbonyl]urea

1-(2-benzoyl-4-chlorophenyl)-3-[(2S)-2-methylpyrrolidine-2-carbonyl]urea

3,4-Dichlorophenylmethyl chloride
102-47-6

3,4-Dichlorophenylmethyl chloride

(S)-N-(2-benzoyl-4-chlorophenyl)-1-(3,4-dichlorobenzyl)-2-methylpyrrolidine-2-carboxamide

(S)-N-(2-benzoyl-4-chlorophenyl)-1-(3,4-dichlorobenzyl)-2-methylpyrrolidine-2-carboxamide

Conditions
ConditionsYield
With potassium hydroxide In dichloromethane at 10 - 30℃;95%
hexamethylenetetramine
100-97-0

hexamethylenetetramine

3,4-Dichlorophenylmethyl chloride
102-47-6

3,4-Dichlorophenylmethyl chloride

N-(3,4-dichlorobenzyl)hexamethylenetetramine chloride
96433-36-2

N-(3,4-dichlorobenzyl)hexamethylenetetramine chloride

Conditions
ConditionsYield
In ethyl acetate at 15 - 75℃; for 6h; Solvent; Temperature;94.8%
Indole-3-carboxaldehyde
487-89-8

Indole-3-carboxaldehyde

3,4-Dichlorophenylmethyl chloride
102-47-6

3,4-Dichlorophenylmethyl chloride

1-(3,4-dichlorobenzyl)-1H-indole-3-carbaldehyde
90815-02-4

1-(3,4-dichlorobenzyl)-1H-indole-3-carbaldehyde

Conditions
ConditionsYield
With sodium hydride 1.) DMF, 2.) DMF, room temp., 15 h;93%
With potassium carbonate In N,N-dimethyl-formamide at 80℃;
With potassium carbonate In N,N-dimethyl-formamide at 80℃;
With sodium hydride In acetonitrile at 20℃; for 4h;
With potassium carbonate In N,N-dimethyl-formamide at 80℃;
isovanillin
621-59-0

isovanillin

3,4-Dichlorophenylmethyl chloride
102-47-6

3,4-Dichlorophenylmethyl chloride

3-(3,4-dichloro-benzyloxy)-4-methoxy-benzaldehyde

3-(3,4-dichloro-benzyloxy)-4-methoxy-benzaldehyde

Conditions
ConditionsYield
With potassium carbonate; sodium iodide In acetonitrile Heating;93%
3,4-Dichlorophenylmethyl chloride
102-47-6

3,4-Dichlorophenylmethyl chloride

8-chloro-[1,2,4]triazolo[4,3-a]pyridine-3(2H)-thione
22841-91-4

8-chloro-[1,2,4]triazolo[4,3-a]pyridine-3(2H)-thione

8-chloro-3-((3,4-dichlorobenzyl)thio)-[1,2,4]triazolo[4,3-a]pyridine

8-chloro-3-((3,4-dichlorobenzyl)thio)-[1,2,4]triazolo[4,3-a]pyridine

Conditions
ConditionsYield
With sodium hydroxide In N,N-dimethyl-formamide at 90℃; for 0.25h; Microwave irradiation;93%
With sodium hydroxide In N,N-dimethyl-formamide at 90℃; for 0.25h; Microwave irradiation;81%
3,4-Dichlorophenylmethyl chloride
102-47-6

3,4-Dichlorophenylmethyl chloride

phenylacetylene
536-74-3

phenylacetylene

C15H11Cl2N3

C15H11Cl2N3

Conditions
ConditionsYield
With sodium azide In water at 70℃; for 7h; Huisgen Cycloaddition; Green chemistry; regioselective reaction;93%
4-bromo-2,6-naphthyridin-1-(2H)-one

4-bromo-2,6-naphthyridin-1-(2H)-one

3,4-Dichlorophenylmethyl chloride
102-47-6

3,4-Dichlorophenylmethyl chloride

C15H9BrCl2N2O

C15H9BrCl2N2O

Conditions
ConditionsYield
With caesium carbonate In N,N-dimethyl-formamide at 20℃;93%
3,4-Dichlorophenylmethyl chloride
102-47-6

3,4-Dichlorophenylmethyl chloride

N-(2,6-dimethylphenyl)-2-(piperazin-1-yl)acetamide
5294-61-1

N-(2,6-dimethylphenyl)-2-(piperazin-1-yl)acetamide

2-(4-(3,4-dichlorobenzyl)piperazin-1-yl)-N-(2,6-dimethylphenyl)acetamide

2-(4-(3,4-dichlorobenzyl)piperazin-1-yl)-N-(2,6-dimethylphenyl)acetamide

Conditions
ConditionsYield
With potassium carbonate In acetonitrile at 25℃; for 10h;93%
3,4-Dichlorophenylmethyl chloride
102-47-6

3,4-Dichlorophenylmethyl chloride

3-Diethylamino-2,3-dihydro-isoindol-1-one
93679-82-4

3-Diethylamino-2,3-dihydro-isoindol-1-one

2-(3,4-Dichloro-benzyl)-3-diethylamino-2,3-dihydro-isoindol-1-one

2-(3,4-Dichloro-benzyl)-3-diethylamino-2,3-dihydro-isoindol-1-one

Conditions
ConditionsYield
With sodium hydroxide; tetra-(n-butyl)ammonium iodide In water; benzene at 60℃; for 0.25h;92%
3,4-Dichlorophenylmethyl chloride
102-47-6

3,4-Dichlorophenylmethyl chloride

L-proline
147-85-3

L-proline

(S)-N-(3,4-dichlorobenzyl)proline
511544-19-7

(S)-N-(3,4-dichlorobenzyl)proline

Conditions
ConditionsYield
Stage #1: 3,4-Dichlorophenylmethyl chloride; L-proline With potassium hydroxide In isopropyl alcohol at 40℃; for 6h;
Stage #2: With hydrogenchloride In water; isopropyl alcohol at 0 - 5℃; pH=5 - 6;
92%
Stage #1: 3,4-Dichlorophenylmethyl chloride; L-proline With isopropyl alcohol; potassium hydroxide at 40℃;
Stage #2: With hydrogenchloride
85%
With potassium hydroxide In isopropyl alcohol at 20℃; for 15h;70%
Stage #1: L-proline With potassium hydroxide In isopropyl alcohol at 39 - 42℃; for 0.333333h;
Stage #2: 3,4-Dichlorophenylmethyl chloride In isopropyl alcohol at 39 - 45℃; for 4h;
1-benzhydryl-3-(4-chlorobenzyloxy)azetidine
232599-02-9

1-benzhydryl-3-(4-chlorobenzyloxy)azetidine

1-(diphenylmethyl)-3-hydroxyazetidine
18621-17-5

1-(diphenylmethyl)-3-hydroxyazetidine

3,4-Dichlorophenylmethyl chloride
102-47-6

3,4-Dichlorophenylmethyl chloride

3-(3,4-Dichlorobenzyloxy)-1-(diphenylmethyl)azetidine
232599-04-1

3-(3,4-Dichlorobenzyloxy)-1-(diphenylmethyl)azetidine

Conditions
ConditionsYield
92%
3,4-Dichlorophenylmethyl chloride
102-47-6

3,4-Dichlorophenylmethyl chloride

N,N-dimethylthiourea
534-13-4

N,N-dimethylthiourea

C10H12Cl2N2S

C10H12Cl2N2S

Conditions
ConditionsYield
In ethanol for 10h; Reflux;92%
6-nitro-2(3H)-benzothiazolone
28620-12-4

6-nitro-2(3H)-benzothiazolone

3,4-Dichlorophenylmethyl chloride
102-47-6

3,4-Dichlorophenylmethyl chloride

C14H8Cl2N2O3S

C14H8Cl2N2O3S

Conditions
ConditionsYield
With potassium hydroxide In water; acetone for 24h; Reflux;92%
3,4-Dichlorophenylmethyl chloride
102-47-6

3,4-Dichlorophenylmethyl chloride

2-cyano-1,5,6,7-tetrahydro-4H-indol-4-one
161468-22-0

2-cyano-1,5,6,7-tetrahydro-4H-indol-4-one

1-(3,4-dichlorobenzyl)-4-oxo-4,5,6,7-tetrahydroindole-2-carbonitrile

1-(3,4-dichlorobenzyl)-4-oxo-4,5,6,7-tetrahydroindole-2-carbonitrile

Conditions
ConditionsYield
With potassium iodide; potassium carbonate In N,N-dimethyl-formamide91%
3-methyl-4-nitrophenol
2581-34-2

3-methyl-4-nitrophenol

3,4-Dichlorophenylmethyl chloride
102-47-6

3,4-Dichlorophenylmethyl chloride

1,2-dichloro-4-[(3-methyl-4-nitrophenoxy)methyl]benzene
1335101-86-4

1,2-dichloro-4-[(3-methyl-4-nitrophenoxy)methyl]benzene

Conditions
ConditionsYield
With potassium carbonate In N,N-dimethyl-formamide at 50 - 100℃;91%
carbon monoxide
201230-82-2

carbon monoxide

4-Chlorophenylboronic acid
1679-18-1

4-Chlorophenylboronic acid

3,4-Dichlorophenylmethyl chloride
102-47-6

3,4-Dichlorophenylmethyl chloride

1-(4-chloro-phenyl)-2,3-bis-(3,4-dichloro-phenyl)-propan-1-one

1-(4-chloro-phenyl)-2,3-bis-(3,4-dichloro-phenyl)-propan-1-one

Conditions
ConditionsYield
With potassium dihydrogenphosphate; sodium phosphate; sodium iodide at 100℃; for 6h;91%
Allylthiourea
109-57-9

Allylthiourea

3,4-Dichlorophenylmethyl chloride
102-47-6

3,4-Dichlorophenylmethyl chloride

C11H12Cl2N2S*ClH

C11H12Cl2N2S*ClH

Conditions
ConditionsYield
In ethanol Reflux;90%
3,4-Dichlorophenylmethyl chloride
102-47-6

3,4-Dichlorophenylmethyl chloride

(E)-3-(pyridin-4-ylmethylene)indolin-2-one
128564-78-3

(E)-3-(pyridin-4-ylmethylene)indolin-2-one

(E)-1-(3,4-dichlorobenzyl)-4-((2-oxoindolin-3-ylidene)methyl)pyridinium chloride
1621102-59-7

(E)-1-(3,4-dichlorobenzyl)-4-((2-oxoindolin-3-ylidene)methyl)pyridinium chloride

Conditions
ConditionsYield
In acetonitrile at 60 - 70℃;90%
3-(5-((3,4-dichlorobenzyl)sulfanyl)-1,3,4-oxadiazol-2-yl)-5-nitrophenyl acetate

3-(5-((3,4-dichlorobenzyl)sulfanyl)-1,3,4-oxadiazol-2-yl)-5-nitrophenyl acetate

3,4-Dichlorophenylmethyl chloride
102-47-6

3,4-Dichlorophenylmethyl chloride

3-(5-((3,4-dichlorobenzyl)sulfanyl)-1,3,4-oxadiazol-2-yl)-5-nitrophenol

3-(5-((3,4-dichlorobenzyl)sulfanyl)-1,3,4-oxadiazol-2-yl)-5-nitrophenol

Conditions
ConditionsYield
With triethylamine In acetonitrile for 1h; Reflux;90%
2-Methylpentane
107-83-5

2-Methylpentane

4-nitro-1H-indole-2-carboxylic acid ethyl ester
4993-93-5

4-nitro-1H-indole-2-carboxylic acid ethyl ester

3,4-Dichlorophenylmethyl chloride
102-47-6

3,4-Dichlorophenylmethyl chloride

Ethyl N-(3,4-dichlorobenzyl)-4-nitroindole-2-carboxylate
220677-29-2

Ethyl N-(3,4-dichlorobenzyl)-4-nitroindole-2-carboxylate

Conditions
ConditionsYield
With potassium iodide; potassium carbonate In N,N-dimethyl-formamide89%
With potassium iodide; potassium carbonate In N,N-dimethyl-formamide89%
3,5-dimethyl-1H-pyrazole
67-51-6

3,5-dimethyl-1H-pyrazole

3,4-Dichlorophenylmethyl chloride
102-47-6

3,4-Dichlorophenylmethyl chloride

1-(3,4-dichlorobenzyl)-3,5-dimethyl-1H-pyrazole
1274494-85-7

1-(3,4-dichlorobenzyl)-3,5-dimethyl-1H-pyrazole

Conditions
ConditionsYield
Stage #1: 3,5-dimethyl-1H-pyrazole With potassium hydroxide In dimethyl sulfoxide at 80℃; for 1h; Inert atmosphere;
Stage #2: 3,4-Dichlorophenylmethyl chloride In dimethyl sulfoxide at 20℃; for 2h; Inert atmosphere;
89%
2-(piperidine-1ylcarbonyl)-6,7-dihydropyrazole[1,5-a]pyrazin-4(5H)-one

2-(piperidine-1ylcarbonyl)-6,7-dihydropyrazole[1,5-a]pyrazin-4(5H)-one

3,4-Dichlorophenylmethyl chloride
102-47-6

3,4-Dichlorophenylmethyl chloride

5-(3,4-dichlorobenzyl)-2-(piperidin-1-ylcarbonyl)-6,7-dihydropyrazolo{1,5-a}pyrazin-4(5H)-one

5-(3,4-dichlorobenzyl)-2-(piperidin-1-ylcarbonyl)-6,7-dihydropyrazolo{1,5-a}pyrazin-4(5H)-one

Conditions
ConditionsYield
Stage #1: 2-(piperidine-1ylcarbonyl)-6,7-dihydropyrazole[1,5-a]pyrazin-4(5H)-one With sodium hydride at 0 - 20℃; for 0.25h;
Stage #2: 3,4-Dichlorophenylmethyl chloride at 0 - 20℃; for 15h;
89%

3,4-Dichlorobenzyl chloride Chemical Properties

IUPAC Name: 1,2-Dichloro-4-(chloromethyl)benzene 
Following is the structure of 3,4-Dichlorobenzyl chloride (CAS NO.102-47-6):
                
Molecular formula: C7H5Cl3
Molecular Weight: 195.47
EINECS: 203-033-0
Index of Refraction: 1.563
Molar Refractivity: 45.8 cm3
Molar Volume: 141 cm3
Density: 1.386 g/cm3
Flash Point: 160.2 °C
Melting point: -3 °C
Polarizability: 18.15 10-24cm3
Surface Tension: 39.8 dyne/cm
Enthalpy of Vaporization: 45.86 kJ/mol
Boiling Point: 241 °C at 760 mmHg
Vapour Pressure: 0.057 mmHg at 25 °C
Appearance of 3,4-Dichlorobenzyl chloride (CAS NO.102-47-6): Clear to yellowish liquid
Canonical SMILES: C1=CC(=C(C=C1CCl)Cl)Cl
InChI: InChI=1S/C7H5Cl3/c8-4-5-1-2-6(9)7(10)3-5/h1-3H,4H2
InChIKey: YZIFVWOCPGPNHB-UHFFFAOYSA-N

3,4-Dichlorobenzyl chloride Uses

 3,4-Dichlorobenzyl chloride (CAS NO.102-47-6) is used as an intermediate in the production of a number of products, including agricultural chemicals, dyes and pigments and pharmaceuticals.

3,4-Dichlorobenzyl chloride Toxicity Data With Reference

 3,4-Dichlorobenzyl chloride (CAS NO.102-47-6) hasn't been listed as a carcinogen by ACGIH, IARC, NTP, or CA Prop 65. And the toxicological properties have not been fully investigated.

3,4-Dichlorobenzyl chloride Safety Profile

Hazard Codes: CorrosiveC
Risk Statements: 34-36/37 
R34:Causes burns. 
R36/37:Irritating to eyes and respiratory system.
Safety Statements: 26-36/37/39-45 
S26: In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. 
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection. 
S45:In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.)
RIDADR UN: 3265 8/PG 2
WGK Germany: 3
F: 19
Hazard Note: Corrosive
HazardClass: 8
PackingGroup: III
HS Code: 29036990

3,4-Dichlorobenzyl chloride Specification

 3,4-Dichlorobenzyl chloride , its cas register number 102-47-6. It also can be called 1,2-Dichloro-4-(chloromethyl)benzene ; AI3-14887 ; NSC 406893 ; and alpha,3,4-Trichlorotoluene .
 3,4-Dichlorobenzyl chloride (CAS NO.102-47-6) is moisture sensitive. It should avoid the condition like incompatible materials, exposure to moist air or water. It is not compatible with water, bases, alcohols, aluminum, amines, iron, steel, Attacks some plastics, rubber and coatings. And also prevent it to broken down into hazardous decomposition products: hydrogen chloride, carbon monoxide, carbon dioxide. However, its hazardous polymerization may occur.

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