3-Bromobenzyl alcohol

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Names

[ CAS No. ]:
15852-73-0

[ Name ]:
3-Bromobenzyl alcohol

[Synonym ]:
RARECHEM AL BD 0052
3-bromo-benzyl alcohol
MFCD00004629
(3-Bromophenyl)methanol
Benzenemethanol,3-bromo
EINECS 239-975-4
Benzenemethanol, 3-bromo-
3-Bromobenzenemethanol
m-bromobenzyl alcohol
3-Bromobenzyl alcohol
3-Bromo benzylalcohol

Chemical & Physical Properties

[ Density]:
1.6±0.1 g/cm3

[ Boiling Point ]:
287.2±0.0 °C at 760 mmHg

[ Melting Point ]:
110-112

[ Molecular Formula ]:
C7H7BrO

[ Molecular Weight ]:
187.034

[ Flash Point ]:
115.7±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

MSDS

Click to get detail MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves

[ Hazard Codes ]:
Xi: Irritant;

[ Safety Phrases ]:
S24/25

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
29062900

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

  • 3-Bromobenzaldehyde
  • QVR CE
  • Ethyl 3-bromobenzoate
  • 3-Bromobenzyl bromide
  • 3-Bromobenzamide
  • Sulfuric acid
  • Methanol
  • Carbon tetrachloride

DownStream

  • diethyl 2-(3-bromobenzyl)Malonate
  • (3-Ethynylphenyl)methanol
  • 3-(3-Bromophenyl)propanoic acid
  • 3-Bromobenzaldehyde
  • QVR CE
  • 5-Bromoindanone
  • 3-(Hydroxymethyl)benzonitrile
  • 3-(hydroxymethyl)benzoic acid
  • 3-(Hydroxymethyl)phenylboronic acid
  • 3-Bromobenzyl bromide

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

Synthesis and biological evaluation of a series of aromatic bisphosphonates.

Bioorg. Med. Chem. 18 , 7212-7220, (2010)

Geminal bisphosphonates display varied biological activity depending on the nature of the substituents on the central carbon atom. For example, the nitrogenous bisphosphonates zoledronate and risedron...

Iridium catalysed alkylation of 4-hydroxy coumarin, 4-hydroxy-2-quinolones and quinolin-4 (1H)-one with alcohols under solvent free thermal conditions. Grigg R, et al.

Tetrahedron 65(36) , 7468-7473, (2009)


More Articles

Related Compounds

  • 3-Bromobenzyl alcohol tetrahydropyranyl ether
  • (3-Bromobenzyl)-cyanoacetic acid
  • (3-BROMOBENZYL)-(1-PHENYLETHYL)AMINE
  • 3-Bromobenzyl isothiocyanate
  • 3-BROMOBENZYL-(CIS-2-PENTENYL)ETHER
  • [(3-BROMOBENZYL)AMINO]ACETIC ACID
  • 2-[(3,4-Difluorophenyl)formamido]-4-methylpentanoic acid
  • N-(4-(N-(4,6-dimethylpyrimidin-2-yl)sulfamoyl)phenyl)-1-((4-fluorobenzyl)oxy)-2-oxo-1,2-dihydropyridine-3-carboxamide
  • 6,8-Dimethoxy-4-quinolinecarboxaldehyde
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