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P4607

Sigma-Aldrich

1,4-Pentadiene

99%

Synonym(s):

Allylethylene

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About This Item

Linear Formula:
CH2=CHCH2CH=CH
CAS Number:
591-93-5
Molecular Weight:
68.12
Beilstein:
1696934
EC Number:
209-736-9
MDL number:
MFCD00008665
UNSPSC Code:
12352100
PubChem Substance ID:
24898557
NACRES:
NA.22

vapor pressure

11.91 psi ( 20 °C)

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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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

Pictograms

FlameHealth hazard
GHS02,GHS08

Signal Word

Danger

Hazard Statements

H224,H304

Hazard Classifications

Asp. Tox. 1 - Flam. Liq. 1

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

-4.0 °F - closed cup

Flash Point(C)

-20 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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
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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