125903
1,3-Dibromopropane
99%, liquid, ReagentPlus®
Synonym(s):
Trimethylene dibromide
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About This Item
Linear Formula:
Br(CH2)3Br
CAS Number:
Molecular Weight:
201.89
NACRES:
NA.21
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
203-690-3
MDL number:
Beilstein/REAXYS Number:
635662
Assay:
99%
Form:
liquid
Product Name
1,3-Dibromopropane, ReagentPlus®, 99%
vapor density
7 (vs air)
Quality Level
product line
ReagentPlus®
assay
99%
form
liquid
refractive index
n20/D 1.524 (lit.)
bp
167 °C (lit.)
mp
−34 °C (lit.)
density
1.989 g/mL at 25 °C (lit.)
SMILES string
BrCCCBr
InChI
1S/C3H6Br2/c4-2-1-3-5/h1-3H2
InChI key
VEFLKXRACNJHOV-UHFFFAOYSA-N
General description
1,3-Dibromopropane is a dihalogenated propane. It undergoes reduction catalyzed by electrogenerated solution-phase nickel(I) salen and nickel(I) salen confined in a polymer film on the surface of a carbon electrode to afford cyclopropane and propylene, respectively.
Application
1,3-Dibromopropane may be used in the preparation of chiral geminal dicationic ionic liquid and 1,3-bis(1-7′-chloro-4-quinolyl-4- piperazinyl)propane.3
Legal Information
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
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Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Chronic 2 - Flam. Liq. 3 - Skin Irrit. 2
Storage Class
3 - Flammable liquids
wgk
WGK 2
flash_point_f
129.2 °F - closed cup
flash_point_c
54 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
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Catalytic reduction of α,ω-dihaloalkanes with nickel (I) salen as a homogeneous-phase and polymer-bound mediator.
Dahm CE and Peters DG.
Journal of Electroanalytical Chemistry, 406(1), 119-129 (1996)
Synthesis of Chiral Geminal Dicationic Ionic Liquid from Amino Acids.
Yin A, et al.
Asian Journal of Chemistry, 25(12), 6721-6721 (2013)
A Witkowski et al.
The Journal of biological chemistry, 267(26), 18488-18492 (1992-09-15)
Thioesterase II is a 29-kDa monomer which, in certain specialized tissues, acts as a chain terminator in fatty acid synthesis by hydrolyzing medium-chain fatty acids from the fatty acid synthase. As with serine proteases, hydrolysis appears to involve acylation of