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1-Octene, 1,1-dichloro- is an organic chemical compound with the molecular formula C8H14Cl2. It is a colorless liquid with a pungent odor and is used as a synthetic intermediate in the production of various chemicals, including pharmaceuticals and agrochemicals. 1-Octene, 1,1-dichloro- is characterized by its octene backbone, which consists of an eight-carbon chain with a double bond between the first and second carbon atoms, and two chlorine atoms attached to the terminal carbon atom. Due to its reactivity and potential health and environmental risks, it is important to handle 1-Octene, 1,1-dichloro- with proper safety measures and in accordance with relevant regulations.

1119-82-0

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1119-82-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1119-82-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,1 and 9 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1119-82:
(6*1)+(5*1)+(4*1)+(3*9)+(2*8)+(1*2)=60
60 % 10 = 0
So 1119-82-0 is a valid CAS Registry Number.

1119-82-0Relevant academic research and scientific papers

Carbanions phosphonate prepares par voie electrochimique: formation et reactivite vis-a-vis d'un aldehyde

Le Menn, Jean-Christophe,Sarrazin, Jean,Tallec, Andre

, p. 1332 - 1343 (2007/10/02)

Reactivity towards p-methoxybenzaldehyde (ArCHO) of electrochemically generated phosphonate carbanions has been investigated.Electrolyses were carried out at a mercury cathode in DMF and two routes to the desired carbanion have been compared: (i) Deprotonation of phosphonates of general formula (EtO)2P(O)CHYW (Y = W = Cl; Y = H, W = Cl; Y = Cl, W = CO2Et; Y = H, W = CO2Et; Y = CH3, W = CO2Et; Y = Cl, W = CH3), by the bases resulting from the electroreduction of azobenzene; addition of the carbanion formed onto the carbonyl group takes place and leads to the adduct (EtO)2P(O)CYW(Ar)O-. (ii) Two-electron reduction of halophosphonates (EtO)2P(O)CXYW (X = Cl, Y and W as above; X = Br, W = CO2Et, Y = Cl, Br, or CH3); when no H atom is present on the carbon bearing the phosphonate group (Y and W no = H), the same evolution leading to the above adduct is observed, on the contrary, when Y = H, the electrogenerated carbanion deprotonates the substrate and the resulting carbanion (EtO)2P(O)CXW reacts with the aldehyde; giving the adduct (EtO)2P(O)CXW(Ar)O-.Evolution of the intermediate adduct depends on the substituents Y (or X) and W: when W = CO2Et, whatever the nature of Y (or X), diethyl phosphate is eliminated with formation of the ethylenic ArCH=CWY (or X) (Wittig-Horner reaction); the same evolution is observed when Y = W = Cl.When W = Cl and Y = H or CH3, the final product is the phosphonate epoxyde resulting from chloride elimination (Darzens reaction).Chemo- and stereoselectivity depend only on the nature of Y and W but are independent of the mode of generation of the carbanion.Yields are limited by side-protonation reactions, which are related to the basicity of the phosphonate carbanions.Analysis of the results permits selection of the optimal electrolysis conditions for purposes of synthesis.Key words: electrosynthesis, electrogenerated bases, phosphonates, Wittig-Horner.

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