<Suppliers Price>

2-Bromobenzyl alcohol

Names

[ CAS No. ]:
18982-54-2

[ Name ]:
2-Bromobenzyl alcohol

[Synonym ]:
o-bromo-benzyl alcohol
2-Br-Ph-CH2OH
2-Bromobenzyl alcohol
EINECS 242-719-4
(2-bromophenyl)methan-1-ol
Benzyl alcohol, o-bromo-
MFCD00004600
(2-Bromophenyl)methanol
ortho-bromobenzyl alcohol
Benzenemethanol, 2-bromo-
2-BrC6H4CH2OH
Benzenemethanol,2-bromo

Chemical & Physical Properties

[ Density]:
1.6±0.1 g/cm3

[ Boiling Point ]:
261.8±15.0 °C at 760 mmHg

[ Melting Point ]:
78-80 °C(lit.)

[ Molecular Formula ]:
C7H7BrO

[ Molecular Weight ]:
187.034

[ Flash Point ]:
112.1±20.4 °C

[ Exact Mass ]:
185.968018

[ PSA ]:
20.23000

[ LogP ]:
1.81

[ Vapour Pressure ]:
0.0±0.6 mmHg at 25°C

[ Index of Refraction ]:
1.592

[ Storage condition ]:
Store at RT.

MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H302-H319

[ Precautionary Statements ]:
P305 + P351 + P338

[ Personal Protective Equipment ]:
Eyeshields;Gloves

[ Hazard Codes ]:
Xi: Irritant;

[ Risk Phrases ]:
52/53

[ Safety Phrases ]:
S24/25

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
29062900

Synthetic Route

Precursor & DownStream

Customs

[ HS Code ]: 2906299090

[ Summary ]:
2906299090 other aromatic alcohols。Supervision conditions:None。VAT:17.0%。Tax rebate rate:9.0%。MFN tariff:5.5%。General tariff:30.0%

Articles

Syntheses of imidazo-, oxa-, and thiazepine ring systems via ring-opening of aziridines/Cu-catalyzed C-N/C-C bond formation.

J. Org. Chem. 79(14) , 6468-79, (2014)

A simple and unpredicted synthetic pathway toward racemic and scalemic tetrahydrodibenzoimidazoazepines has been invented serendipitously proceeding through an S(N)2-type ring-opening of N-activated a...

Fast microwave promoted palladium-catalyzed synthesis of phthalides from bromobenzyl alcohols utilizing DMF and Mo (CO)6 as carbon monoxide sources. Wu X, et al.

Tetrahedron Lett. 45(24) , 4635-38, (2004)

Synthesis and structure of benzoboroxoles: novel organoboron heterocycles. Zhdankin VV, et al.

Tetrahedron Lett. 40(37) , 6705-8, (1999)


More Articles


Related Compounds