4714-15-2 Usage
General Description
p-(β-Chlorophenethyl)toluene is a chemical compound that belongs to the class of toluene derivatives. It is primarily used as an intermediate in the production of various chemicals, including pharmaceuticals, agrochemicals, and fragrances. p-(β-Chlorophenethyl)toluene is a derivative of toluene, with a beta-chlorophenethyl group attached to the para-position of the toluene ring. It has applications in the synthesis of organic compounds and is widely used in chemical research and development. The compound has potential uses as a building block in the development of new drugs and other bioactive molecules due to its specific molecular structure. However, it is important to handle this compound with care, as it can present hazards if not used and stored properly.
Check Digit Verification of cas no
The CAS Registry Mumber 4714-15-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,7,1 and 4 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4714-15:
(6*4)+(5*7)+(4*1)+(3*4)+(2*1)+(1*5)=82
82 % 10 = 2
So 4714-15-2 is a valid CAS Registry Number.
4714-15-2Relevant articles and documents
Palladium-catalyzed oxidative arylhalogenation of alkenes: Synthetic scope and mechanistic insights
Kalyani, Dipannita,Satterfield, Andrew D.,Sanford, Melanie S.
supporting information; experimental part, p. 8419 - 8427 (2010/08/04)
This article describes the development of a Pd-catalyzed reaction for the arylhalogenation (halogen = Cl or Br) of diverse α-olefins by oxidatively intercepting Mizoroki-Heck intermediates. These transformations afford synthetically useful 1,2- and 1,1-arylhalogenated products in good yields with good to excellent selectivities that can be modulated by changing the nature of the halogenating reagent and/or the reaction conditions. The selectivity of these reactions can be rationally tuned by (i) controlling the relative rates of oxidative functionalization versus β-hydride elimination from equilibrating PdII-alkyl species and (ii) stabilization of organometallic PdII intermediates through the formation of π-benzyl adducts. These arylhalogenations exhibit modest to excellent levels of stereoselectivity, and the key carbon-halogen bond-forming step proceeds with predominant retention of stereochemistry at carbon.
