Methyl 3-bromobenzoate
Suppliers
Names
[ CAS No. ]:
618-89-3
[ Name ]:
Methyl 3-bromobenzoate
[Synonym ]:
3-methoxycarbonyl-1-bromobenzene
(3-bromophenyl)acetic acid methyl ester
m-bromobenzoic acid methyl ester
Methyl 3-bromobenzoate
Benzoic acid, m-bromo-, methyl ester
MFCD00017777
Benzoic acid,3-bromo-,methyl ester
Methyl-3-brombenzolcarboxylat
Benzoic acid, 3-bromo-, methyl ester
methyl-3-bromobenzoate
Methyl m-bromobenzoate
EINECS 210-569-9
3-MeO2CC6H4Br
3-Bromobenzoic acid,methyl ester
Chemical & Physical Properties
[ Density]:
1.5±0.1 g/cm3
[ Boiling Point ]:
244.4±13.0 °C at 760 mmHg
[ Melting Point ]:
31-33 °C(lit.)
[ Molecular Formula ]:
C8H7BrO2
[ Molecular Weight ]:
215.044
[ Flash Point ]:
101.6±19.8 °C
[ Exact Mass ]:
213.962936
[ PSA ]:
26.30000
[ LogP ]:
2.88
[ Vapour Pressure ]:
0.0±0.5 mmHg at 25°C
[ Index of Refraction ]:
1.550
[ Storage condition ]:
Room temperature.
MSDS
Safety Information
[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
[ Hazard Codes ]:
Xi:Irritant;
[ Risk Phrases ]:
R36/37/38
[ Safety Phrases ]:
S37/39-S26
[ RIDADR ]:
NONH for all modes of transport
[ WGK Germany ]:
3
[ HS Code ]:
2916399090
Synthetic Route
Precursor & DownStream
Precursor
DownStream
Customs
[ HS Code ]: 2916399090
[ Summary ]:
2916399090 other aromatic monocarboxylic acids, their anhydrides, halides, peroxides, peroxyacids and their derivatives VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:30.0%
Articles
Chemistry 18(10) , 2978-86, (2012)
Dichloro[bis{1-(dicyclohexylphosphanyl)piperidine}]palladium [(P{(NC(5)H(10))(C(6)H(11))(2)})(2)PdCl(2)] (1) is a highly active and generally applicable C-C cross-coupling catalyst. Apart from its hig...
Science 345(6195) , 433-6, (2014)
The routine application of C(sp3)-hybridized nucleophiles in cross-coupling reactions remains an unsolved challenge in organic chemistry. The sluggish transmetalation rates observed for the preferred ...
Negishi cross-coupling reaction catalyzed by an aliphatic, phosphine based pincer complex of palladium. biaryl formation via cationic pincer-type PdIV intermediates. Gerber R, et al.Dalton Trans. 40(35) , 8996-9003, (2011)