92552-87-9 Usage
Molecular weight
257.31 g/mol
The mass of one mole of 2-(4-methoxy-phenyl)-4H-benzo[1,4]thiazin-3-one is 257.31 grams.
Physical appearance
Yellow crystalline powder
The compound appears as a yellow, crystalline solid in powder form.
Solubility
Insoluble in water, soluble in organic solvents (e.g., ethanol, dimethyl sulfoxide)
The compound does not dissolve in water but dissolves in certain organic solvents like ethanol and dimethyl sulfoxide.
Structure
Benzothiazine ring system with a methoxyphenyl group at the 2-position
The compound has a core structure consisting of a benzothiazine ring, with a methoxyphenyl group attached to the second position of the ring.
Family
Thiazinone
2-(4-methoxy-phenyl)-4H-benzo[1,4]thiazin-3-one belongs to the thiazinone family of compounds, which are known for their potential pharmaceutical applications.
Pharmaceutical potential
Anti-inflammatory and antimicrobial properties
The compound has been studied for its potential use in pharmaceuticals, particularly for its ability to reduce inflammation and inhibit the growth of microorganisms.
Check Digit Verification of cas no
The CAS Registry Mumber 92552-87-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,5,5 and 2 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 92552-87:
(7*9)+(6*2)+(5*5)+(4*5)+(3*2)+(2*8)+(1*7)=149
149 % 10 = 9
So 92552-87-9 is a valid CAS Registry Number.
92552-87-9Relevant articles and documents
Expeditious synthesis of C2- or N4-aryl-1,4-benzothiazin-3-one via orthogonal Pd-catalyzed C-arylation and Cu-catalyzed N-arylation
Huang, Wei-Sheng,Xu, Rongsong,Dodd, Rory,Shakespeare, William C.
, p. 441 - 444 (2014/01/06)
Direct, chemo-specific arylation at C-2 or N-4 of 1,4-benzothiazin-3-one with aryl halides, based on Pd or Cu catalyst system, respectively, provided easy entry to arylated derivatives, a class of molecules not easily accessible via existing methods. Under Pd-catalysis conditions with LiHMDS as the base, N-arylation of 1,4-benzothiazin-3-one was inhibited leading to Cα-arylation of a secondary amide without the need for protection and de-protection of more acidic amido NH.
A novel, convenient synthesis of 2-Aryl-3-oxo-3,4-dihydro-2H-1,4-benzothiazines
Fujita,Ota,Ito,Yamamoto,Kawashima
, p. 599 - 604 (2007/10/02)
-
