All Photos(1)
Synonym(s):
Allylethylene
Linear Formula:
CH2=CHCH2CH=CH
CAS Number:
Molecular Weight:
68.12
Beilstein:
1696934
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
vapor pressure
11.91 psi ( 20 °C)
Quality Level
Assay
99%
refractive index
n20/D 1.389 (lit.)
bp
26 °C (lit.)
mp
−148 °C (lit.)
density
0.659 g/mL at 25 °C (lit.)
storage temp.
2-8°C
SMILES string
C=CCC=C
InChI
1S/C5H8/c1-3-5-4-2/h3-4H,1-2,5H2
InChI key
QYZLKGVUSQXAMU-UHFFFAOYSA-N
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Related Categories
Application
1,4-Pentadiene can be used as a precursor in the synthesis of (+)-isolysergol, phosphorinanes and lithium pentadienyl complexes.
accessory
Product No.
Description
Pricing
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Asp. Tox. 1 - Flam. Liq. 1
WGK
WGK 3
Flash Point(F)
closed cup
Flash Point(C)
closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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Fethi Khaled et al.
The journal of physical chemistry. A, 123(11), 2261-2271 (2019-02-16)
Hydroxyl radicals and olefins are quite important from a combustion and an atmospheric chemistry standpoint. Large amounts of olefinic compounds are emitted into the earth's atmosphere from both biogenic and anthropogenic sources. Olefins make a significant share in transportation fuels
Light-Driven, Zirconium-Catalyzed Hydrophosphination with Primary Phosphines.
Bange C A, et al.
ACS Catalysis (2018)
A H Neerincx et al.
Journal of breath research, 10(4), 046014-046014 (2016-12-03)
Staphylococcus aureus (S. aureus) is a common bacterium infecting children with cystic fibrosis (CF). Since current detection methods are difficult to perform in children, there is need for an alternative. This proof of concept study investigates whether breath profiles can
Jason A Deck et al.
Organic letters, 12(11), 2610-2613 (2010-05-14)
The first enantioselective synthesis of (+)-isolysergol was completed in 12 steps from commercially available materials by a novel approach that features a late stage microwave-mediated, diastereomeric ring-closing metathesis catalyzed by a chiral molybdenum catalyst to simultaneously form the D ring
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