382043
Benzyl 3-bromopropyl ether
98%
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About This Item
Linear Formula:
C6H5CH2O(CH2)3Br
CAS Number:
Molecular Weight:
229.11
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Product Name
Benzyl 3-bromopropyl ether, 98%
InChI
1S/C10H13BrO/c11-7-4-8-12-9-10-5-2-1-3-6-10/h1-3,5-6H,4,7-9H2
SMILES string
BrCCCOCc1ccccc1
InChI key
PSUXTZLDBVEZTD-UHFFFAOYSA-N
assay
98%
form
liquid
refractive index
n20/D 1.531 (lit.)
bp
130-132 °C/8 mmHg (lit.)
density
1.298 g/mL at 25 °C (lit.)
functional group
bromo
ether
phenyl
Quality Level
Related Categories
Application
Benzyl 3-bromopropyl ether may be used in the following studies:
- Preparation of (2S,3S)-1-[(triisopropylsilyl)oxy]-7-(benzyloxy)-2,3-(isopropylidenedioxy)-4(Z)-heptene.
- Preparation of 5-(3-Benzyloxypropoxy)psoralen (PAP-7).
- Total synthesis of zincophorin and (+)-anatoxin-a.
General description
Benzyl 3-bromopropyl ether is an ether.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2
Storage Class
10 - Combustible liquids
wgk
WGK 3
flash_point_f
235.4 °F - closed cup
flash_point_c
113 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
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Magali Defosseux et al.
The Journal of organic chemistry, 69(14), 4626-4647 (2004-07-03)
A total synthesis of the naturally occurring ionophore zincophorin has been realized. The route features an intramolecular oxymercuration of a cyclopropanemethanol and a Carroll-Claisen rearrangement for the respective elaboration of the C1-C12 and C13-C25 subunits, which have been assembled by
Tetrahedron Letters, 45, 4397-4399 (2004)
Alexander Schmitz et al.
Molecular pharmacology, 68(5), 1254-1270 (2005-08-16)
The lymphocyte K+ channel Kv1.3 constitutes an attractive pharmacological target for the selective suppression of terminally differentiated effector memory T (TEM) cells in T cell-mediated autoimmune diseases, such as multiple sclerosis and type 1 diabetes. Unfortunately, none of the existing
Synthesis of natural and modified trapoxins, useful reagents for exploring histone deacetylase function.
Taunton J, et al.
Journal of the American Chemical Society, 118(43), 10412-10422 (1996)
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