| Identification | More | [Name]
3-Chlorobenzyl bromide | [CAS]
766-80-3 | [Synonyms]
1-(bromomethyl)-3-chlorobenzene
3-CHLOROBENZYL BROMIDE
A-BROMO-M-CHLOROTOLUENE
ALPHA-BROMO-3-CHLOROTOLUENE
ALPHA-BROMO-M-CHLOROTOLUENE
M-CHLOROBENZYL BROMIDE
Toluene, alpha-bromo-m-chloro-
α-Bromo-3-chlorotoluene
3-CHLOROBENZYL BROMIDE 95% (GC)
3-Chlorobenzylbromide,97%
3-Chlorobenzyl bromide, 98+%
Benzene, 1-(bromomethyl)-3-chloro-
à-bromo-3-chlorotoluene
3-Chlorobenzyl bromide 97%
A-BROMO-3-CHLOROTOLUENE
m-Chloro-α-bromotoluene
α-Bromo-m-chlorotoluene | [EINECS(EC#)]
212-171-0 | [Molecular Formula]
C7H6BrCl | [MDL Number]
MFCD00000597 | [Molecular Weight]
205.48 | [MOL File]
766-80-3.mol |
| Chemical Properties | Back Directory | [Appearance]
Colorless liquid | [Melting point ]
15 °C | [Boiling point ]
109-110 °C/12 mmHg (lit.) | [density ]
1.565 g/mL at 25 °C(lit.)
| [refractive index ]
n20/D 1.588(lit.)
| [Fp ]
>230 °F
| [storage temp. ]
Store at R.T. | [form ]
powder to lump to clear liquid | [color ]
White or Colorless to Yellow | [Specific Gravity]
1.565 | [Water Solubility ]
DECOMPOSES | [Sensitive ]
Lachrymatory | [Detection Methods]
GC | [BRN ]
636504 | [CAS DataBase Reference]
766-80-3(CAS DataBase Reference) | [NIST Chemistry Reference]
Benzene, 1-(bromomethyl)-3-chloro-(766-80-3) | [Storage Precautions]
Store under nitrogen |
| Safety Data | Back Directory | [Hazard Codes ]
C | [Risk Statements ]
R34:Causes burns. | [Safety Statements ]
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 label where possible) . | [RIDADR ]
UN 3265 8/PG 2
| [WGK Germany ]
3
| [F ]
19 | [Hazard Note ]
Corrosive/Lachrymatory | [HazardClass ]
6.1 | [PackingGroup ]
III | [HS Code ]
29039990 |
| Hazard Information | Back Directory | [Chemical Properties]
Colorless liquid | [Uses]
3-Chlorobenzyl bromide was used in the synthesis of symmetrical and unsymmetrical benzyl thioethers. It was used as starting reagent during the synthesis of 1-(3-chlorobenzyl)-2-(pyrrolidin-1-ylmethyl)-1H-benzimidazole dihydrochloride. | [General Description]
3-Chlorobenzyl bromide reacts with aminoethanol and NaH to yield aminoethyl 3-chlorobenzyl ether. |
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