167169
3-Bromo-1-propanol
97%
Synonym(s):
Trimethylene bromohydrin
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About This Item
Linear Formula:
Br(CH2)3OH
CAS Number:
Molecular Weight:
138.99
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
210-986-6
Beilstein/REAXYS Number:
969160
MDL number:
Assay:
97%
Form:
liquid
Quality Level
assay
97%
form
liquid
refractive index
n20/D 1.488 (lit.)
bp
62 °C/5 mmHg (lit.)
density
1.537 g/mL at 25 °C (lit.)
functional group
bromo, hydroxyl
storage temp.
2-8°C
SMILES string
OCCCBr
InChI
1S/C3H7BrO/c4-2-1-3-5/h5H,1-3H2
InChI key
RQFUZUMFPRMVDX-UHFFFAOYSA-N
General description
Reaction between 3-bromo-1-propanol, phenol and a series of phenols having substituents in 4-position has been studied in micellar media and in microemulsions based on cationic or a nonionic surfactant.
3-Bromo-1-propanol is an electrophile used as a substrate in nucleophilic substitution reactions and in the redox polymerization.
3-Bromo-1-propanol is an electrophile used as a substrate in nucleophilic substitution reactions and in the redox polymerization.
Application
3-Bromo-1-propanol was used in the synthesis of fluorescent halide-sensitive quinolinium dyes and molten salt-polymers. It was used in the synthesis of chiral, quaternary prolines via cyclization of quaternary amino acids.
Recently used as a grafting agent in the synthesis of recyclable reagents for Swern oxidation
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1
Storage Class
10 - Combustible liquids
wgk
WGK 3
flash_point_f
149.0 °F - closed cup
flash_point_c
65 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
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Use of self-assembled surfactant systems as media for a substitution reaction
Fredrik and Currie
Journal of Colloid and Interface Science, 277, 230-234 (2004)
Wei Song et al.
Molecules (Basel, Switzerland), 25(17) (2020-08-23)
Azobenzene (AB) units were successfully introduced into poly(1,6-heptadiyne)s in order to ensure smooth synthesis of double- and single-stranded poly(1,6-heptadiyne)s (P1 and P2) and simultaneously realize the self-assembly by Grubbs-III catalyst-mediated metathesis cyclopolymerization (CP) of AB-functionalized bis(1,6-heptadiyne) and 1,6-heptadiyne monomers (M1
Fredrik Currie
Journal of colloid and interface science, 277(1), 230-234 (2004-07-28)
The reaction between 3-bromo-1-propanol and phenol and a series of phenols carrying substituents in 4-position was studied in micellar media and in microemulsions based on either a cationic or a nonionic surfactant. The reactivity and the yield were evaluated and
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 167169-100G | 04061838749390 |
| 167169-25G | 04061838749406 |
| 167169-5G | 04061838749413 |