Conditions | Yield |
---|---|
With sulfuryl dichloride; dibenzoyl peroxide | |
With chlorine | |
With chlorine |
Conditions | Yield |
---|---|
With iodine beim Chlorieren; |
Conditions | Yield |
---|---|
With hydrogenchloride; zinc(II) chloride |
chloromethyl methyl ether
1,2-dichloro-benzene
3,4-Dichlorophenylmethyl chloride
Conditions | Yield |
---|---|
With sulfuric acid |
Conditions | Yield |
---|---|
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; |
Conditions | Yield |
---|---|
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 |
Conditions | Yield |
---|---|
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
1-(azidomethyl)-3,4-dichlorobenzene
Conditions | Yield |
---|---|
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
3,4-Dichlorophenylmethyl chloride
Conditions | Yield |
---|---|
With potassium carbonate In acetonitrile for 18h; Reflux; | 100% |
3,4-Dichlorophenylmethyl chloride
2,2'-iminobis[ethanol]
2-[(2-Hydroxy-ethyl)-(3,4-dichloro-benzyl)-amino]-ethanol
Conditions | Yield |
---|---|
With potassium carbonate In acetone for 8h; Heating; | 99% |
99% | |
99% |
3,4-Dichlorophenylmethyl chloride
6-methanesulphonyl-2(3H)-benzoxazolone
3-(3,4-dichlorobenzyl)-6-methanesulphonyl-2(3H)-benzoxazolone
Conditions | Yield |
---|---|
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% |
Conditions | Yield |
---|---|
With caesium carbonate In N,N-dimethyl-formamide at 20℃; for 24h; | 98% |
Conditions | Yield |
---|---|
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
3,4-Dichlorophenylmethyl chloride
3-({5-chloro-2-[1-naphthylthio]phenyl}amino)-N-(3,4-dichlorobenzyl)-N,N-dimethylpropan-1-ammonium chloride
Conditions | Yield |
---|---|
In acetone at 120℃; for 0.333333h; Inert atmosphere; Microwave irradiation; | 97% |
Conditions | Yield |
---|---|
With potassium carbonate; potassium iodide In acetone at 60℃; for 24h; Inert atmosphere; | 95% |
3,4-Dichlorophenylmethyl chloride
Conditions | Yield |
---|---|
With potassium hydroxide In dichloromethane at 10 - 30℃; | 95% |
hexamethylenetetramine
3,4-Dichlorophenylmethyl chloride
N-(3,4-dichlorobenzyl)hexamethylenetetramine chloride
Conditions | Yield |
---|---|
In ethyl acetate at 15 - 75℃; for 6h; Solvent; Temperature; | 94.8% |
Indole-3-carboxaldehyde
3,4-Dichlorophenylmethyl chloride
1-(3,4-dichlorobenzyl)-1H-indole-3-carbaldehyde
Conditions | Yield |
---|---|
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℃; |
Conditions | Yield |
---|---|
With potassium carbonate; sodium iodide In acetonitrile Heating; | 93% |
3,4-Dichlorophenylmethyl chloride
8-chloro-[1,2,4]triazolo[4,3-a]pyridine-3(2H)-thione
Conditions | Yield |
---|---|
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% |
Conditions | Yield |
---|---|
With sodium azide In water at 70℃; for 7h; Huisgen Cycloaddition; Green chemistry; regioselective reaction; | 93% |
Conditions | Yield |
---|---|
With caesium carbonate In N,N-dimethyl-formamide at 20℃; | 93% |
3,4-Dichlorophenylmethyl chloride
N-(2,6-dimethylphenyl)-2-(piperazin-1-yl)acetamide
Conditions | Yield |
---|---|
With potassium carbonate In acetonitrile at 25℃; for 10h; | 93% |
3,4-Dichlorophenylmethyl chloride
3-Diethylamino-2,3-dihydro-isoindol-1-one
Conditions | Yield |
---|---|
With sodium hydroxide; tetra-(n-butyl)ammonium iodide In water; benzene at 60℃; for 0.25h; | 92% |
3,4-Dichlorophenylmethyl chloride
L-proline
(S)-N-(3,4-dichlorobenzyl)proline
Conditions | Yield |
---|---|
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
1-(diphenylmethyl)-3-hydroxyazetidine
3,4-Dichlorophenylmethyl chloride
3-(3,4-Dichlorobenzyloxy)-1-(diphenylmethyl)azetidine
Conditions | Yield |
---|---|
92% |
Conditions | Yield |
---|---|
In ethanol for 10h; Reflux; | 92% |
Conditions | Yield |
---|---|
With potassium hydroxide In water; acetone for 24h; Reflux; | 92% |
3,4-Dichlorophenylmethyl chloride
2-cyano-1,5,6,7-tetrahydro-4H-indol-4-one
Conditions | Yield |
---|---|
With potassium iodide; potassium carbonate In N,N-dimethyl-formamide | 91% |
3-methyl-4-nitrophenol
3,4-Dichlorophenylmethyl chloride
1,2-dichloro-4-[(3-methyl-4-nitrophenoxy)methyl]benzene
Conditions | Yield |
---|---|
With potassium carbonate In N,N-dimethyl-formamide at 50 - 100℃; | 91% |
carbon monoxide
4-Chlorophenylboronic acid
3,4-Dichlorophenylmethyl chloride
Conditions | Yield |
---|---|
With potassium dihydrogenphosphate; sodium phosphate; sodium iodide at 100℃; for 6h; | 91% |
Conditions | Yield |
---|---|
In ethanol Reflux; | 90% |
3,4-Dichlorophenylmethyl chloride
(E)-3-(pyridin-4-ylmethylene)indolin-2-one
(E)-1-(3,4-dichlorobenzyl)-4-((2-oxoindolin-3-ylidene)methyl)pyridinium chloride
Conditions | Yield |
---|---|
In acetonitrile at 60 - 70℃; | 90% |
3,4-Dichlorophenylmethyl chloride
Conditions | Yield |
---|---|
With triethylamine In acetonitrile for 1h; Reflux; | 90% |
2-Methylpentane
4-nitro-1H-indole-2-carboxylic acid ethyl ester
3,4-Dichlorophenylmethyl chloride
Ethyl N-(3,4-dichlorobenzyl)-4-nitroindole-2-carboxylate
Conditions | Yield |
---|---|
With potassium iodide; potassium carbonate In N,N-dimethyl-formamide | 89% |
With potassium iodide; potassium carbonate In N,N-dimethyl-formamide | 89% |
3,5-dimethyl-1H-pyrazole
3,4-Dichlorophenylmethyl chloride
1-(3,4-dichlorobenzyl)-3,5-dimethyl-1H-pyrazole
Conditions | Yield |
---|---|
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% |
3,4-Dichlorophenylmethyl chloride
Conditions | Yield |
---|---|
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% |
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 (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 (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.
Hazard Codes: C
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 , 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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