Basic information
- CAS
622-95-7- Standard SMILES
Clc1ccc(CBr)cc1- InChIKey
KQNBRMUBPRGXSL-UHFFFAOYSA-N- Molecular formula
- C7H6BrCl
- Average molar mass
- 205.48 g/mol
- Monoisotopic mass
- 203.93413997
Names & identifiers
- Preferred name
- 1-(Bromomethyl)-4-chlorobenzene
- IUPAC
- 1-(bromomethyl)-4-chlorobenzene
- English name
- 4-Chlorobenzyl bromide
- Molecular formula
- C7H6BrCl
- Molecular weight
- 205.48
Names & synonyms
Show more names
Database identifiers
- CAS
622-95-7- PubChem CID
- 69329
- DTXSID
DTXSID70211247- UNII
- RAN8LE8F5N
- EC Number
- 210-760-7
- Nikkaji
- J95.366K
Properties
Computed structural properties
- XLogP
- 3.4
- Topological polar surface area
- 0 Ų
- Hydrogen bond donors
- 0
- Hydrogen bond acceptors
- 0
- Rotatable bonds
- 1
- Heavy atoms
- 9
- Formal charge
- 0
- Complexity
- 77
Experimental & physicochemical properties
Physicochemical properties
- Melting point
- 48 · 48-52 °C (lit.)
- Boiling point
- 107 · 107-108°C 8mm
- Density
- 1.57 · 1.570±0.06 g/cm3(Predicted)
- Flash point
- 230 °F · >230 °F
- storage temp.
- 2 · Inert atmosphere,2-8°C
- solubility
- Chloroform, Dichloromethane (Slightly)
- form
- Crystalline Low Melting Solid
- color
- White
- Water Solubility
- Insoluble in water.
- Sensitive
- Lachrymatory
- BRN
- 606497 · 606497
- InChI
- InChI=1S/C7H6BrCl/c8-5-6-1-3-7(9)4-2-6/h1-4H,5H2
- InChIKey
- KQNBRMUBPRGXSL-UHFFFAOYSA-N
- SMILES
- C1(CBr)=CC=C(Cl)C=C1
- CAS DataBase Reference
- 622 · 622-95-7(CAS DataBase Reference)
- FDA UNII
- 8 LE8F5N · RAN8LE8F5N
- NIST Chemistry Reference
- 4 · 4-Chlorobenzyl bromide(622-95-7)
- UNSPSC Code
- 12352100 · 12352100
- NACRES
- 22 · NA.22
- Symbol(GHS)
- 5 · GHS05
- Signal word
- Danger
- Hazard statements
- 314 · H314
- Precautionary statements
- 260 · P260-P280-P303+P361+P353-P304+P340+P310-P305+P351+P338-P363
- PPE
- 3 · Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
- Hazard Codes
- C
- Risk Statements
- 34 · 34
- Safety Statements
- 26 · 26-36/37/39-45
- RIDADR
- 1759 · UN 1759 8/PG 2
- WGK Germany
- 3 · 3
- Hazard Note
- Corrosive/Lachrymatory
- HazardClass
- 6.1 · 6.1
- PackingGroup
- II
- HS Code
- 29049090 · 29049090
- Storage Class
- 8 A · 8A - Combustible corrosive hazardous materials
- Hazard Classifications
- 1 B · Skin Corr. 1B
- Limited Quantities
- 1 Kg · 1 Kg (2.2 lbs) (solid)
- Excepted Quantities
- Max Inner Pack (30g or 30ml) and Max Outer Pack (500g or 500ml)
Safety & regulation
GHS classification
GHS Classification
Danger
H314 (100%): Causes severe skin burns and eye damage [Danger Skin corrosion/irritation]
P260, P264, P280, P301+P330+P331, P302+P361+P354, P304+P340, P305+P354+P338, P316, P321, P363, P405, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 48 reports by companies from 4 notifications to the ECHA C&L Inventory.
Hazard information
Safety data
- PPE
- Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
- wgk
- 3
- ridadr
- UN 1759 8/PG 2
- hs_code
- 29049090
- risk_code
- 34
- Signal word
- Danger
- Symbol(GHS)
- GHS05
- hazard_code
- C
- hazard_note
- Corrosive/Lachrymatory
- safety_code
- 26-36/37/39-45
- hazard_class
- 6.1
- Storage Class
- 8A - Combustible corrosive hazardous materials
- packing_group
- II
- Hazard statements
- H314
- Limited Quantities
- 1 Kg (2.2 lbs) (solid)
- Excepted Quantities
- Max Inner Pack (30g or 30ml) and Max Outer Pack (500g or 500ml)
- Hazard Classifications
- Skin Corr. 1B
- Precautionary statements
- P260-P280-P303+P361+P353-P304+P340+P310-P305+P351+P338-P363
Chemistry & industry
Applications
Uses4-Chlorobenzyl bromide is used as pharmaceutical intermediate.
Uses4-Chlorobenzyl bromide may be used to synthesize 1-(4-chlorobenzyl)-2-(pyrrolidin-1-yl-methyl)-1H-benzimidazole dihydrochloride
General Description4-Chlorobenzyl bromide undergoes carbonylation in the presence of dimer of chloro(1,5-cyclooctadiene)rhodium(I) to yield the corresponding phenylacetic acid. It can be synthesized by reacting 4-chlorobenzyl alcohol with bromodimethylsulfonium bromide (BDMS) It can also be synthesized by refluxing a mixture of 4-chlorobenzaldehyde, chlorotrimethylsilane, 1,1,3,3-tetramethyldisiloxane and lithium bromide.
Upstream & downstream products
Downstream products
Suppliers100 total
Related reactions
Compound notes
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