165806-95-1 Usage
Description
A-(P-TOLUENESULFONYL)-4-FLUOROBENZYLISONITRILE, also known as Alpha-(p-toluenesulfonyl)-4-fluorobenzylisonitrile, is an organic compound with the chemical formula C14H10FNO2S. It is a derivative of benzylisonitrile, featuring a p-toluenesulfonyl and a 4-fluorophenyl group. A-(P-TOLUENESULFONYL)-4-FLUOROBENZYLISONITRILE is known for its potential applications in various chemical and pharmaceutical processes due to its unique structural properties.
Uses
Used in Chemical Synthesis:
A-(P-TOLUENESULFONYL)-4-FLUOROBENZYLISONITRILE is used as a synthetic reagent for the development of novel functionalized imidazoles. Its unique structure allows for the creation of new compounds with potential applications in various industries, including pharmaceuticals and materials science.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, A-(P-TOLUENESULFONYL)-4-FLUOROBENZYLISONITRILE is used as a key intermediate in the synthesis of various drug candidates. Its ability to form novel imidazoles makes it a valuable component in the development of new medications with potential therapeutic benefits.
Used in DNA-Compatible Methods:
A-(P-TOLUENESULFONYL)-4-FLUOROBENZYLISONITRILE is also used as a reagent in the development of DNA-compatible methods. These methods are essential for the study and manipulation of DNA, which can lead to advancements in genetic research, gene therapy, and the development of new diagnostic tools.
Check Digit Verification of cas no
The CAS Registry Mumber 165806-95-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,5,8,0 and 6 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 165806-95:
(8*1)+(7*6)+(6*5)+(5*8)+(4*0)+(3*6)+(2*9)+(1*5)=161
161 % 10 = 1
So 165806-95-1 is a valid CAS Registry Number.
InChI:InChI=1/C15H12FNO2S/c1-11-3-9-14(10-4-11)20(18,19)15(17-2)12-5-7-13(16)8-6-12/h3-10,15H,1H3
165806-95-1Relevant articles and documents
The base-free van Leusen reaction of cyclic imines on water: Synthesis of N-fused imidazo 6,11-dihydro β-carboline derivatives
Satyam, Killari,Murugesh,Suresh, Surisetti
, p. 5234 - 5238 (2019/06/07)
Construction of imidazoles has been demonstrated on water under base-free conditions. The reaction of dihydro β-carboline imines and p-toluenesulfonylmethyl isocyanides furnished the corresponding substituted N-fused imidazo 6,11-dihydro β-carboline derivatives in very good yields under ambient conditions. The use of deuterium oxide (D2O) as a solvent enabled the incorporation of deuterium isotopes in the imidazole ring.
1,3-DIARYL-SUBSTITUTED HETEROCYCLIC PESTICIDES
-
, (2013/12/03)
Disclosed are compounds of Formula 1, N-oxides, and salts thereof, wherein Q is and Z1, Z2, J1, J2, M, R1a, R1b, R2a, R2b, R2c, R2d, R14/su
BENZIMIDAZOLES AND BENZOTHIAZOLES AS INHIBITORS OF MAP KIANSE
-
Page 27, (2010/11/30)
-