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29570

Sigma-Aldrich

1,3-Cyclooctadiene

technical, ≥95% (GC)

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About This Item

Empirical Formula (Hill Notation):
C8H12
CAS Number:
1700-10-3
Molecular Weight:
108.18
Beilstein:
2321915
EC Number:
216-929-1
MDL number:
MFCD00001751
UNSPSC Code:
12352100
PubChem Substance ID:
57648378
NACRES:
NA.22

grade

technical

Assay

≥95% (GC)

refractive index

n20/D 1.494

bp

142-144 °C (lit.)

density

0.873 g/mL at 20 °C (lit.)

storage temp.

2-8°C

SMILES string

C1CCC=CC=CC1

InChI

1S/C8H12/c1-2-4-6-8-7-5-3-1/h1-4H,5-8H2/b3-1-,4-2-

InChI key

RRKODOZNUZCUBN-CCAGOZQPSA-N

Related Categories

General description

Enantiodifferentiating geometrical photoisomerizations of (Z,Z)-1,3-cyclooctadiene was studied using "cyclodextrin nanosponge", as a supramolecular sensitizing host. Dendrimer-encapsulated Pd-Rh bimetallic nanoparticle catalyzed partial hydrogenation of 1,3-cyclooctadiene has been reported.

Application

1,3-Cyclooctadiene has been used in the preparation of 2-cyclooct-2-en-1-yl-1,3-cyclooctadiene, a novel bicyclic triene.

Pictograms

FlameHealth hazard
GHS02,GHS08

Signal Word

Danger

Hazard Statements

H226,H304

Precautionary Statements

P210 - P301 + P310 + P331

Hazard Classifications

Asp. Tox. 1 - Flam. Liq. 3

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

77.0 °F - closed cup

Flash Point(C)

25 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

FSL

Group 4: Flammable liquids
Type 2 petroleums
Hazardous rank III
Water insoluble liquid

JAN Code

29570-250ML:
29570-VAR:
29570-10ML:
29570-BULK:
29570-50ML:

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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Metal-mediated dimerization of 1, 3-cyclooctadiene to 2-cyclooct-2-en-1-yl-1, 3-cyclooctadiene: a novel bicyclic triene.
Debad JD, et al.
Journal of the American Chemical Society, 115(5), 2051-2052 (1993)
Wenting Liang et al.
Beilstein journal of organic chemistry, 8, 1305-1311 (2012-09-29)
Enantiodifferentiating geometrical photoisomerizations of (Z)-cyclooctene and (Z,Z)-1,3-cyclooctadiene were performed by using the pyromellitate-linked cyclodextrin network polymer, termed "cyclodextrin nanosponge (CDNS)", as a supramolecular sensitizing host. The photochirogenic behavior of the nanosponges incorporating β- or γ-cyclodextrin was significantly different from that
Partial hydrogenation of 1, 3-cyclooctadiene using dendrimer-encapsulated Pd-Rh bimetallic nanoparticles.
Chung Y-M and Rhee H-K.
J. Mol. Catal. A: Chem., 206(1), 291-298 (2003)

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