P4607
1,4-Pentadiene
99%
Synonym(s):
Allylethylene
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About This Item
Linear Formula:
CH2=CHCH2CH=CH
CAS Number:
Molecular Weight:
68.12
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
209-736-9
Beilstein/REAXYS Number:
1696934
MDL number:
Assay:
99%
InChI key
QYZLKGVUSQXAMU-UHFFFAOYSA-N
InChI
1S/C5H8/c1-3-5-4-2/h3-4H,1-2,5H2
SMILES string
C=CCC=C
vapor pressure
11.91 psi ( 20 °C)
assay
99%
Quality Level
bp
26 °C (lit.)
mp
−148 °C (lit.)
density
0.659 g/mL at 25 °C (lit.)
storage temp.
2-8°C
Related Categories
Application
1,4-Pentadiene can be used as a precursor in the synthesis of (+)-isolysergol, phosphorinanes and lithium pentadienyl complexes.
signalword
Danger
hcodes
Hazard Classifications
Asp. Tox. 1 - Flam. Liq. 1
Storage Class
3 - Flammable liquids
wgk
WGK 3
flash_point_f
-4.0 °F - closed cup
flash_point_c
-20 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves
Regulatory Information
监管及禁止进口产品
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Fethi Khaled et al.
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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
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Light-Driven, Zirconium-Catalyzed Hydrophosphination with Primary Phosphines.
Bange C A, et al.
ACS Catalysis (2018)
Structural Influences in Lithium Pentadienylsilane Complexes.
Day B M, et al.
Organometallics, 32(15), 4448-4451 (2013)
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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