7,7-Dichlorobicyclo[3.2.0]hept-2-en-6-one
![7,7-Dichlorobicyclo[3.2.0]hept-2-en-6-one Structure](CAS/GIF/5307-99-3.gif)
- CAS No.
- 5307-99-3
- Chemical Name:
- 7,7-Dichlorobicyclo[3.2.0]hept-2-en-6-one
- Synonyms
- NSC 116987;Dichlorobicycloheptenone;Prostaglandin Impurity 4;7,7-Dichloro[3.2.0]hept-2-en-6-one;7,7-DICHLOROBICYCLO[3.2.0]HEPT-2-ENONE;7,7-DICHLOROBICYCLO[3.2.0]HEPT-2-EN-6-ONE;6,6-dichlorobicyclo[3.2.0]hept-3-en-7-one;7,7-DICHLOROBICYCLO[3.2.0]HEPT-2-ENE-6-ONE;7,7-Dichloro-6-oxobicyclo[3.2.0]hept-2-ene;Bicyclo[3.2.0]hept-2-en-6-one, 7,7-dichloro-
- CBNumber:
- CB0472056
- Molecular Formula:
- C7H6Cl2O
- Molecular Weight:
- 177.03
- MOL File:
- 5307-99-3.mol
- Modify Date:
- 2023/4/23 13:52:06
Boiling point | 58-64 °C (0.5 mmHg) |
---|---|
Density | 1.44±0.1 g/cm3(Predicted) |
refractive index | 1.5150 |
Flash point | 127-128°C/25mm |
storage temp. | Refrigerator (+4°C) |
form | liquid |
color | Clear, dark orange |
BRN | 2045059 |
CAS DataBase Reference | 5307-99-3(CAS DataBase Reference) |
SAFETY
Risk and Safety Statements
Symbol(GHS) | ![]() ![]() GHS05,GHS07 |
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Signal word | Danger | |||||||||
Hazard statements | H315-H319-H302-H314 | |||||||||
Precautionary statements | P280-P305+P351+P338-P310-P264-P280a-P321-P332+P313-P337+P313 | |||||||||
Hazard Codes | Xi,C | |||||||||
Risk Statements | 36/37/38-34-22 | |||||||||
Safety Statements | 26-36/37/39-45 | |||||||||
RIDADR | UN 3265 8 / PGIII | |||||||||
WGK Germany | 2 | |||||||||
Hazard Note | Irritant | |||||||||
HS Code | 2914290090 | |||||||||
NFPA 704 |
|
7,7-Dichlorobicyclo[3.2.0]hept-2-en-6-one Chemical Properties,Uses,Production
Chemical Properties
clear brown liquid
Synthesis
Under nitrogen protection, to a solution of dichloracetyl chloride (34 g, 0.23 mol) and cyclopentadiene(60 ml, 0.7 mol) in pentane (230 ml), heated to reflux in a three-necked flask with constant pressure funnel and condenser tube, was added dropwise via funnel triethylamine (24 g, 0.24 mol) in pentane (100 ml) with mechanical stirring during 4 hours, and a lot of white triethylamine hydrochloride was produced. After reflux for 2 hours, water (80 ml) was added to dissolve the triethylamine hydrochloride. The reaction mixture was extracted with pentane (2 × 60ml). The combined extracts were filtered and dried over anhydrous Na2SO4, and concentrated in vacuo to give brownish black oil. Fraction of reduced pressure distillation at 83~87 °C/400 Pa was collected to give 7,7-Dichlorobicyclo[3.2.0]hept-2-en-6-one (2, 33.5 g) as a colorless oil.
7,7-Dichlorobicyclo[3.2.0]hept-2-en-6-one Preparation Products And Raw materials
Raw materials
Preparation Products
Supplier | Tel | Country | ProdList | Advantage | Inquiry |
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VladaChem GmbH | +49-7246-3082843 | Germany | 1859 | 58 | Inquiry |
LEAPCHEM CO., LTD. | +86-852-30606658 | China | 43340 | 58 | Inquiry |
Shandong Liteng Biotechnology Co. , Ltd. | +86-18663721413 +86-15552573001 | China | 1143 | 58 | Inquiry |
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