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About This Item
Linear Formula:
C6H5CH2O(CH2)4OH
CAS Number:
Molecular Weight:
180.24
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
1944253
Assay:
97%
InChI
1S/C11H16O2/c12-8-4-5-9-13-10-11-6-2-1-3-7-11/h1-3,6-7,12H,4-5,8-10H2
SMILES string
OCCCCOCc1ccccc1
InChI key
TYROJDFHUXSBHC-UHFFFAOYSA-N
assay
97%
Quality Level
bp
216-256 °C (lit.)
density
1.025 g/mL at 25 °C (lit.)
functional group
ether, hydroxyl, phenyl
Related Categories
General description
4-Benzyloxy-1-butanol can be prepared starting from butane-1,4-diol.
Application
4-Benzyloxy-1-butanol may be used for the preparation of ethyl 6-benzyloxy-2-hexenoate, via Swern oxidation and Wadsworth-Emmons olefination. It may be used as starting reagent for the synthesis of 4-(benzyloxy)butanal.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
10 - Combustible liquids
wgk
WGK 3
flash_point_f
228.2 °F - closed cup
flash_point_c
109 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
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The syntheses of tricyclic analogues of O 6-methylguanine.
Hammond DM, et al.
Organic & Biomolecular Chemistry, 1(23), 4166-4172 (2003)
Improved preparation of ?-hydroxy-a-amino acids: direct formation of sulfates by sulfuryl chloride.
Alonso M and Riera M.
Tetrahedron Asymmetry, 16(23), 3908-3912 (2005)
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