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N-(quinolin-3-yl)-4-methylbenzenesulfonamide is a chemical compound with the molecular formula C16H14N2O2S. It is a derivative of benzenesulfonamide, featuring a quinoline-3-yl group attached to the nitrogen atom and a methyl group on the para position of the benzene ring. N-(quinolin-3-yl)-4-methylbenzenesulfonamide is known for its potential applications in the field of medicinal chemistry, particularly as a building block for the synthesis of various pharmaceuticals and agrochemicals. Its structure allows for the exploration of different biological activities, making it a subject of interest for researchers in drug discovery and development.

7101-92-0

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Basic information
1. Product Name: N-(quinolin-3-yl)-4-methylbenzenesulfonamide
2. Synonyms: N-(quinolin-3-yl)-4-methylbenzenesulfonamide
3. CAS NO:7101-92-0
4. Molecular Formula:
5. Molecular Weight: 298.365
6. EINECS: N/A
7. Product Categories: N/A
Chemical Properties
1. Melting Point: N/A
2. Boiling Point: N/A
3. Flash Point: N/A
4. Appearance: N/A
5. Density: N/A
6. Refractive Index: N/A
7. Storage Temp.: N/A
8. Solubility: N/A
9. CAS DataBase Reference: N-(quinolin-3-yl)-4-methylbenzenesulfonamide(CAS DataBase Reference)
10. NIST Chemistry Reference: N-(quinolin-3-yl)-4-methylbenzenesulfonamide(7101-92-0)
11. EPA Substance Registry System: N-(quinolin-3-yl)-4-methylbenzenesulfonamide(7101-92-0)
Safety Data
1. Hazard Codes: N/A
2. Statements: N/A
3. Safety Statements: N/A
4. WGK Germany:
5. RTECS:
6. HazardClass: N/A
7. PackingGroup: N/A
8. Hazardous Substances Data: 7101-92-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 7101-92-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,0 and 1 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 7101-92:
(6*7)+(5*1)+(4*0)+(3*1)+(2*9)+(1*2)=70
70 % 10 = 0
So 7101-92-0 is a valid CAS Registry Number.

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7101-92-0Relevant academic research and scientific papers

SYNTHESIS OF 2,3-FUSED QUINOLINES FROM 3-SUBSTITUTED QUINOLINE 1-OXIDES. PART 1.

Miura, Yutaka,Takaku, Sakae,Fujimura, Yasuo,Hamana, Masatomo

, p. 1055 - 1063 (1992)

3-(2-Bromoethyltosylamino)quinoline 1-oxide (4) reacted with TsCl-NH4OH and TsCl-K2CO3 to afford the 2-aminoquinoline (5) and the 2-quinoline (8).Cyclization of 5 and 8 under basic conditions gave the piperazino-quinoline (6) and the morpholino-quinoline

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