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187895

Sigma-Aldrich

3-Bromobenzyl alcohol

99%

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About This Item

Linear Formula:
BrC6H4CH2OH
CAS Number:
15852-73-0
Molecular Weight:
187.03
EC Number:
239-975-4
MDL number:
MFCD00004629
UNSPSC Code:
12352100
PubChem Substance ID:
24851291
NACRES:
NA.22

Assay

99%

form

liquid

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

SMILES string

OCc1cccc(Br)c1

InChI

1S/C7H7BrO/c8-7-3-1-2-6(4-7)5-9/h1-4,9H,5H2

InChI key

FSWNRRSWFBXQCL-UHFFFAOYSA-N

Application

3-Bromobenzyl alcohol was employed in the preparation of tert-butyl 3-(3-bromophenyl)-2-cyanopropanoate and silyl ether.

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BGBB7389
43196JJV
43196JJ
27996EJ
01202KE

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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)
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

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