6641-15-2 Usage
Molecular structure
2-(3-nitrophenyl)-2,3-dihydro-1H-naphtho[1,2-e][1,3]oxazine has a complex molecular structure with a heterocyclic ring containing nitrogen and oxygen atoms.
Type of compound
It is a type of oxazine, which is a heterocyclic compound containing nitrogen and oxygen atoms in the ring.
Functional group
The presence of a nitrophenyl group in its structure.
Potential use
2-(3-nitrophenyl)-2,3-dihydro-1H-naphtho[1,2-e][1,3]oxazine is likely to be used as a dye or pigment due to the presence of the nitrophenyl group.
Ring system
The dihydro-naphtho ring system in its structure.
Potential applications
It may have potential applications in organic synthesis or pharmaceutical research due to its unique dihydro-naphtho ring system.
Versatility
The compound's unique structure and functional groups make it a versatile and potentially useful chemical in various industrial and scientific applications.
Check Digit Verification of cas no
The CAS Registry Mumber 6641-15-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,4 and 1 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6641-15:
(6*6)+(5*6)+(4*4)+(3*1)+(2*1)+(1*5)=92
92 % 10 = 2
So 6641-15-2 is a valid CAS Registry Number.
6641-15-2Relevant academic research and scientific papers
An efficient one-pot strategies for the synthesis of [1,3] oxazine derivatives
Sapkal, Suryakant B.,Shelke, Kiran F.,Shingate, Bapurao B.,Shingare, Murlidhar S.
experimental part, p. 437 - 442 (2010/10/19)
Sodium hydrogen sulphate (NaHSO4), n-tetra butyl ammonium bromide (TBAB) as a phase transfer catalyst (PTC) in water, and 1-butyl-3-methyl imidazolium hydrogen sulphate [bmim]HSO4 as ionic liquid (IL) has been used as a mild reaction promoter for the cyclocondensation of formalin, β-naphthol and aromatic amines to afford respective 2,3-dihydro-2-phenyl- 1H-naphtho-[1,2-e] [1,3] oxazine derivatives. The present protocols are greener, high yielding and involved the nonchromatographic isolation procedure.
