<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

The content on this webpage is sourced from various professional data sources. If you have any questions or concerns regarding the content, please feel free to contact service1@chemsrc.com.