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:
Assay:
98%
Form:
liquid
Quality Level
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
SMILES string
BrCCCOCc1ccccc1
InChI
1S/C10H13BrO/c11-7-4-8-12-9-10-5-2-1-3-6-10/h1-3,5-6H,4,7-9H2
InChI key
PSUXTZLDBVEZTD-UHFFFAOYSA-N
General description
Benzyl 3-bromopropyl ether is an ether.
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.
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
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)
Tetrahedron Letters, 45, 4397-4399 (2004)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 382043-1G | 04061837008641 |
| 382043-10G | 04061837014895 |