Cas 253602-53-8,Benzenesulfonamide, N-(2-fluorophenyl)-N-(2-hydroxy-3-phenoxypropyl)-4-methyl-

253602-53-8

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Basic information

Product Name: Benzenesulfonamide, N-(2-fluorophenyl)-N-(2-hydroxy-3-phenoxypropyl)-4-methyl-
Synonyms:
CAS NO:253602-53-8
Molecular Formula: C22H22FNO4S
Molecular Weight: 415.485
EINECS: N/A
Product Categories: N/A
Mol File: 253602-53-8.mol

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: Benzenesulfonamide, N-(2-fluorophenyl)-N-(2-hydroxy-3-phenoxypropyl)-4-methyl-(CAS DataBase Reference)
NIST Chemistry Reference: Benzenesulfonamide, N-(2-fluorophenyl)-N-(2-hydroxy-3-phenoxypropyl)-4-methyl-(253602-53-8)
EPA Substance Registry System: Benzenesulfonamide, N-(2-fluorophenyl)-N-(2-hydroxy-3-phenoxypropyl)-4-methyl-(253602-53-8)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 253602-53-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 253602-53-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,3,6,0 and 2 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 253602-53:
(8*2)+(7*5)+(6*3)+(5*6)+(4*0)+(3*2)+(2*5)+(1*3)=118
118 % 10 = 8
So 253602-53-8 is a valid CAS Registry Number.

253602-53-8Upstream product

253602-53-8Downstream Products

253602-55-0 N-Tosyl-2-phenoxymethyl-1,4-benzoxazine

253602-53-8Relevant academic research and scientific papers

Novel concise synthesis of 2-substituted 3,4-dihydro-2H-1,4-benzoxazines by ring opening of glycidols under solid-liquid phase transfer catalysis conditions

Albanese, Domenico,Landini, Dario,Penso, Michele

, p. 2095 - 2096 (2007/10/03)

The ring opening of glycidols with N-(2-fluorophenyl)toluene-p-sulfonamide under SL-PTC conditions, followed by ring closure with Bu(t)OK, provides a novel high yielding synthesis of 2-substituted 3,4-dihydro-2H-1,4-benzoxazines.

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