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3,4-Dibromoanisole

Product Name
3,4-Dibromoanisole
CAS No.
62415-74-1
Chemical Name
3,4-Dibromoanisole
Synonyms
4-Dibromoanisole;3,4-Dibromoanisol;1,2-Dibromo-4-methoxybenzene;Benzene, 1,2-dibromo-4-methoxy-;3,4-Dibromoanisole 94%, remainder predominantly isomer
CBNumber
CB91106771
Molecular Formula
C7H6Br2O
Formula Weight
265.93
MOL File
62415-74-1.mol
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3,4-Dibromoanisole Property

Boiling point:
127℃
Density 
1.823±0.06 g/cm3 (20 ºC 760 Torr)
Flash point:
104.9±20.3℃
storage temp. 
2-8°C
Appearance
Colorless to light yellow Liquid
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Safety

HS Code 
2909309090
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

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N-Bromosuccinimide Price

TRC
Product number
D422978
Product name
3,4-Dibromoanisole
Packaging
1g
Price
$130
Updated
2021/12/16
SynQuest Laboratories
Product number
2607-9-29
Product name
3,4-Dibromoanisole
Packaging
1g
Price
$264
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
HCH0012007
Product name
3,4-DIBROMOANISOLE
Purity
95.00%
Packaging
5MG
Price
$501.72
Updated
2021/12/16
AK Scientific
Product number
V6948
Product name
3,4-Dibromoanisole
Packaging
1g
Price
$26
Updated
2021/12/16
AK Scientific
Product number
J94669
Product name
3,4-Dibromoanisole
Packaging
5g
Price
$60
Updated
2021/12/16
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3,4-Dibromoanisole Chemical Properties,Usage,Production

Synthesis

2398-37-0

62415-74-1

GENERAL METHODS: N-bromosuccinimide (NBS, 1.5 eq., 0.3 mmol), catalyst (10 mol%, 0.02 mmol) and acetonitrile (CH3CN, 1.0 mL) were sequentially added to the reaction tube, followed by m-bromoanisole (0.2 mmol). The reaction mixture was stirred at room temperature for 12 hours away from light. Upon completion of the reaction, the reaction was quenched by the addition of saturated sodium thiosulfate (Na2S2O3) aqueous solution (2 mL). The reaction mixture was extracted with ethyl acetate (3.5 mL). The organic phases were combined, washed with saturated saline (10 mL), dried over anhydrous sodium sulfate (Na2SO4) and filtered through a diatomaceous earth pad. The filtrate was concentrated under reduced pressure and the residue was purified by rapid chromatography on a silica gel column with the eluent of petroleum ether/dichloromethane (5:1, v/v) to afford the target product 3,4-dibromoanisole.

References

[1] Tetrahedron, 2017, vol. 73, # 50, p. 7105 - 7114
[2] Bulletin de la Societe Chimique de France, 1981, vol. 1, # 1-2, p. 42 - 48
[3] Synthetic Communications, 2000, vol. 30, # 12, p. 2091 - 2098

3,4-Dibromoanisole Preparation Products And Raw materials

Raw materials

Preparation Products

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3,4-Dibromoanisole Suppliers

Achemica
Tel
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Fax
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Email
contact@achemica.com
Country
Switzerland
ProdList
6155
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