187895
3-Bromobenzyl alcohol
99%
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About This Item
Linear Formula:
BrC6H4CH2OH
CAS Number:
Molecular Weight:
187.03
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
239-975-4
MDL number:
Assay:
99%
Form:
liquid
form
liquid
InChI key
FSWNRRSWFBXQCL-UHFFFAOYSA-N
InChI
1S/C7H7BrO/c8-7-3-1-2-6(4-7)5-9/h1-4,9H,5H2
SMILES string
OCc1cccc(Br)c1
assay
99%
refractive index
n20/D 1.584 (lit.)
bp
165 °C/16 mmHg (lit.)
density
1.56 g/mL at 25 °C (lit.)
functional group
bromo, hydroxyl
Application
3-Bromobenzyl alcohol was employed in the preparation of tert-butyl 3-(3-bromophenyl)-2-cyanopropanoate and silyl ether.
Storage Class
10 - Combustible liquids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves
Regulatory Information
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Rocky J Barney et al.
Bioorganic & medicinal chemistry, 18(20), 7212-7220 (2010-09-14)
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 risedronate inhibit the enzyme farnesyl diphosphate synthase while digeranyl bisphosphonate has been shown to inhibit
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)
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