14403-01-1 Usage
Description
[3-(chloromethyl)-3-phenyloxiran-2-yl](phenyl)methanone is a complex organic compound characterized by a three-membered oxirane ring, a phenyl group, and a methanone group. The presence of a chlorine atom attached to a carbon atom within the molecule suggests potential reactivity and versatility in various chemical reactions. This unique structure positions the compound as a candidate for applications in organic synthesis, pharmaceuticals, and materials science, warranting further study and investigation.
Uses
Used in Organic Synthesis:
[3-(chloromethyl)-3-phenyloxiran-2-yl](phenyl)methanone is used as an intermediate in the synthesis of various organic compounds due to its reactive functional groups, which can be manipulated to produce a wide range of products.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, [3-(chloromethyl)-3-phenyloxiran-2-yl](phenyl)methanone is used as a building block for the development of new drugs. Its unique structure may contribute to the creation of novel therapeutic agents with specific biological activities.
Used in Materials Science:
[3-(chloromethyl)-3-phenyloxiran-2-yl](phenyl)methanone is used as a component in the development of advanced materials, such as polymers and composites, due to its potential to form covalent bonds and create complex molecular architectures.
Used in Chemical Research:
[3-(chloromethyl)-3-phenyloxiran-2-yl](phenyl)methanone is also used as a subject of study in chemical research to explore its reactivity, stability, and potential applications in various chemical processes and reactions.
Check Digit Verification of cas no
The CAS Registry Mumber 14403-01-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,4,0 and 3 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 14403-01:
(7*1)+(6*4)+(5*4)+(4*0)+(3*3)+(2*0)+(1*1)=61
61 % 10 = 1
So 14403-01-1 is a valid CAS Registry Number.
14403-01-1Relevant articles and documents
Crystal structure of 3-chloromethyl-(3-phenyl-oxiranyl)phenyl methanone: New monoclinic polymorph
Arshad, Muhammad Nadeem,Asiri, Abdullah M.,Alamry, Khalid A.,Al-Juaid, Salih S.,Khan, Sher Bahadar,Bokhari, Tanveer Hussain,Shafiq, Muhammad
, p. 2715 - 2717 (2014/06/09)
The compound, 3-chloromethyl-(3-phenyl-oxiranyl)phenyl methanone [m.f. C16H13O2Cl] was a self-condensation product of phenacyl chloride where the reaction carried out in ethanol medium using inorganic base. This was crystalized in monoclinic with space group P21/c (no. 14), a = 10.1312 (2) ?, b = 11.7728 ?, c = 11.8566 ?, V = 1344.07 ?3, Z = 4 and ρcalc. = 1.348 mg/mm3. The dihedral angle between two aromatic rings is 73.46 (5). The epoxide ring is oriented at dihedral angles of 62.12 (9°) and 60.87 (7°) with respect to the phenyl and benzoyl rings. The non-classical intermolecular hydrogen bonding of C-HO type has been observed in the crystal structure of molecule.
SYNTHESIS AND SOME REACTIONS OF INDOLO-1,4-OXAZINIUM PERCHLORATES
Kibal'nyi, A.V.,Nikolyukin, Yu.A.,Dulenko, V.I.
, p. 895 - 900 (2007/10/02)
The reaction of acyl perchlorates with 1-phenacylskatole affords the previously unknown 1-R-10-methyl-3-phenylindolo-1,4-oxazinium salts, which undergo recyclization by the action of ammonia to the corresponding indolopyrazines.It is found t
