6267-90-9 Usage
General Description
(2,6-dichlorophenyl) (2-propenyl) ether, also known as allyl 2,6-dichlorophenyl ether, is a chemical compound with the molecular formula C9H8Cl2O. It is a colorless to pale yellow liquid with a sharp, pungent odor. (2,6-dichlorophenyl) (2-propenyl) ether is used as a chemical intermediate in the production of pharmaceuticals, fungicides, and other organic compounds. It is also used as a flavoring agent and fragrance ingredient in perfumes and soaps. However, it is important to handle this compound with caution as it can be irritating to the skin, eyes, and respiratory system. Additionally, it is harmful if swallowed, inhaled, or absorbed through the skin, and it may cause adverse effects on human health and the environment if not properly managed and disposed of.
Check Digit Verification of cas no
The CAS Registry Mumber 6267-90-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,6 and 7 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6267-90:
(6*6)+(5*2)+(4*6)+(3*7)+(2*9)+(1*0)=109
109 % 10 = 9
So 6267-90-9 is a valid CAS Registry Number.
InChI:InChI=1/C9H8Cl2O/c1-2-6-12-9-7(10)4-3-5-8(9)11/h2-5H,1,6H2
6267-90-9Relevant articles and documents
Facile one-pot synthesis of aliphatic bridged diaryloxy compounds, cyclic and crown ethers under mild conditions
Sakate, Sachin,Kamble, Sumit,Chikate, Rajiv,Rode, Chandrashekhar
, p. 462 - 470 (2017/03/27)
We report here the facile, room temperature, catalyst free, one pot synthesis of aliphatic bridged diaryloxy compounds, cyclic and crown ethers. Anhydrous potassium carbonate (K2CO3) as a mild base along with dimethyl sulfoxide gener
Intramolecular transition-metal catalyzed cyclizations of electron rich chloroarenes
Braese, Stefan
, p. 6757 - 6759 (2007/10/03)
Electron rich chromium tricarbonylchloroarene complexes bearing an allyl ether moiety were cyclized under palladium catalysis with concomitant loss of the metal carbonyl fragment to give heterocyclic systems in moderate to good yields. Bimetallic catalysis with palladium and chromium compounds gave rise to cyclization of the parent chloroarenes in moderate yields and with low turnover numbers.
