B78106
1-Bromopropane
99%
Synonym(s):
Propyl bromide
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About This Item
Linear Formula:
CH3CH2CH2Br
CAS Number:
Molecular Weight:
122.99
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
203-445-0
Beilstein/REAXYS Number:
505936
MDL number:
Assay:
99%
Form:
liquid
vapor density
4.3 (vs air)
Quality Level
vapor pressure
146 mmHg ( 20 °C)
assay
99%
form
liquid
autoignition temp.
914 °F
refractive index
n20/D 1.434 (lit.)
bp
71 °C (lit.)
mp
−110 °C (lit.)
density
1.354 g/mL at 25 °C (lit.)
SMILES string
CCCBr
InChI
1S/C3H7Br/c1-2-3-4/h2-3H2,1H3
InChI key
CYNYIHKIEHGYOZ-UHFFFAOYSA-N
Application
1-Bromopropane is used as a component of various models of binary mixtures, prepared to study their properties such as viscosity and refractive index.
It can be used as an alkylating reagent:
It can also be used as a reactant:
It can be used as an alkylating reagent:
- For the functionalization of seleno-substituted imidazo[1,2-α]pyridine derivatives.
- For the synthesis of 1,4-dihydroxy-2-propoxy anthraquinone derivatives.
It can also be used as a reactant:
- For the synthesis of Berberine-benzimidazole derivatives.
- For the synthesis of alkyl aryl ketones via carbonylative Barbier-Negishi coupling with aryl iodides.
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signalword
Danger
Hazard Classifications
Aquatic Chronic 3 - Carc. 2 - Eye Irrit. 2 - Flam. Liq. 3 - Ozone 1 - Repr. 1B - Skin Irrit. 2 - STOT RE 2 Inhalation - STOT SE 3
target_organs
Central nervous system, Liver,Central nervous system, Respiratory system
Storage Class
3 - Flammable liquids
wgk
WGK 2
flash_point_f
76.1 °F - closed cup
flash_point_c
24.5 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
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Viscosity of pure organic liquids and binary liquid mixtures (2009)
Design, synthesis and biological evaluation of berberine-benzimidazole hybrids as new type of potentially DNA-targeting antimicrobial agents.
Jeyakkumar P, et al.
European Journal of Medicinal Chemistry, 122(11), 205-215 (2016)
Nickel-catalyzed C (sp2)-H selenation of imidazo [1, 2-?] pyridines with arylboronic acids or alkyl reagents using selenium powder.
Zhu J, et al.
Tetrahedron, 74(45), 6569-6576 (2018)