1,5-CYCLOOCTADIENE

1,5-CYCLOOCTADIENE Structure
CAS No.
1552-12-1
Chemical Name:
1,5-CYCLOOCTADIENE
Synonyms
COD;CIS,CIS-1,5-CYCLOOCTADIENE;(1Z,5Z)-1,5-cyclooctadiene;(1Z,5Z)-cyclooctadiene;1,5-cyclooctadiene(z,z);(Z,Z)-Cycloocta-1,5-dien;(Z,Z)-1,5-Cyclooctadiene;1,5-cyclooctadiene,(Z,Z)-;(Z,Z)-cycloocta-1,5-diene;cis,cis-Cycloocta-1,5-diene
CBNumber:
CB1446850
Molecular Formula:
C8H12
Molecular Weight:
108.18
MOL File:
1552-12-1.mol
Modify Date:
2023/8/14 17:44:59

1,5-CYCLOOCTADIENE Properties

Melting point −69 °C(lit.)
Boiling point 149-150 °C(lit.)
Density 0.882 g/mL at 25 °C(lit.)
vapor pressure 25.8 mm Hg ( 37.7 °C)
refractive index n20/D 1.493
Flash point 89 °F
storage temp. 2-8°C
solubility water: soluble0.05g/L
form Liquid
BRN 1209288
CAS DataBase Reference 1552-12-1(CAS DataBase Reference)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS02,GHS07,GHS08,GHS09
Signal word  Danger
Hazard statements  H226-H302+H332-H304-H411-H302-H315-H317-H319-H332-H335-H401
Precautionary statements  P210-P261-P303+P361+P353-P305+P351+P338-P405-P501a-P273-P301+P310-P331
Hazard Codes  Xn,N
Risk Statements  10-36/38-42/43-65-51/53-20/22
Safety Statements  26-36-62-36/37-23
RIDADR  UN 2520 3/PG 3
WGK Germany  3
RTECS  GX9620000
10-23
TSCA  Yes
HazardClass  3
PackingGroup  III
NFPA 704
2
3 0

1,5-CYCLOOCTADIENE Chemical Properties,Uses,Production

Uses

cis,cis-1,5-Cyclooctadiene (COD) has been employed as ligand:

  • during regio- and stereoselective synthesis of (Z)-1,2-dihaloalkenes
  • in the preparation of metal complexes, e.g. bis-COD-nickel, a versatile reagent for preparing (PI)-allylnickel halides

General Description

Surface grafting of cis,cis-1,5-cyclooctadiene (cyclic olefin) with low strain energy was explored using ring-opening metathesis polymerization in the vapor phase. The inclusion complex of cis,cis-1,5-cyclooctadiene with β-cyclodextrin (β-CD) was studied by using proton NMR spectroscopy.

Purification Methods

Purify it by GLC. It has been purified via the AgNO3 salt. This is prepared by shaking with a solution of 50% aqueous AgNO3 w/w several times (e.g. 3 x 50mLand4x50mL) at 70ofor ca 20minutes to get a good separation of layers. The upper layers are combined and further extracted with AgNO3 at 40o (2 x 20 mL). The upper layer (19 mL) of original hydrocarbon mixture gives colourless needles of the AgNO3 complex on cooling. The adduct is recrystallised from MeOH (and cooling to 0o). The hydrocarbon is recovered by steam distilling the salt. The distillate is extracted with Et2O, dried (MgSO4), filtered, evaporated and distilled. [Jones J Chem Soc 312 1954,[Beilstein 5 H 116, 5 IV 403.]

1,5-CYCLOOCTADIENE Preparation Products And Raw materials

Raw materials

Preparation Products

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(1Z,5Z)-cyclooctadiene (Z,Z)-1,5-Cyclooctadiene 1,5-cyclooctadiene(z,z) 1,5-cyclooctadiene,(Z,Z)- cis,cis-Cycloocta-1,5-diene (Z,Z)-cycloocta-1,5-diene 1,5-Cyclooctadiene, (1Z,5Z)- (Z,Z)-Cycloocta-1,5-dien cis,cis-1,5-Cyclooctadiene, 99%, stab. with 50-200ppm Irganox 1076 cis,cis-1,5-Cyclooctadiene, stab. with 50-200ppm Irganox 1076 cis,cis-1,5-Cyclooctadiene,COD cis,cis-1,5-Cyclooctadiene >=98.0% (GC) cis,cis-1,5-Cyclooctadiene, stabilized with 50 to 200ppm Irganox 1076 (1Z,5Z)-1,5-cyclooctadiene CIS,CIS-1,5-CYCLOOCTADIENE COD 1552-12-1 Building Blocks Alkenes Organic Building Blocks Cyclic