19282-45-2 Usage
General Description
TIMTEC-BB SBB005657, also known as 4-Aminophenylsulfone, is a chemical compound with the molecular formula C6H7NO2S. It is a white crystalline solid that is commonly used as an intermediate in the production of dyes and pharmaceuticals. 4-Aminophenylsulfone is also used as a building block in the synthesis of various organic compounds. It is considered to be stable under normal conditions and is not highly reactive. However, it should be handled with care and stored in a cool, dry place away from sources of ignition. This chemical is not known to be highly toxic, but exposure should be minimized to avoid potential health hazards.
Check Digit Verification of cas no
The CAS Registry Mumber 19282-45-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,2,8 and 2 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 19282-45:
(7*1)+(6*9)+(5*2)+(4*8)+(3*2)+(2*4)+(1*5)=122
122 % 10 = 2
So 19282-45-2 is a valid CAS Registry Number.
InChI:InChI=1/C11H14O2S/c1-2-13-11(12)10-7-8-5-3-4-6-9(8)14-10/h7H,2-6H2,1H3
19282-45-2Relevant articles and documents
Base catalyzed reaction of ethyl thioglycolate with β-aryl-β-(methylthio) acroleins: A general method for the synthesis of 2-carbethoxy-5-substituted/4,5-annulated thiophenes in high overall yields
Byre Gowda,Pradeepa Kumara,Ramesh,Sadashiva,Junjappa
supporting information, p. 928 - 931 (2016/02/05)
(Methylthio) acroleins 1a-m were shown to be stable unlike their counterpart the chloroacroleins and their efficacy as 1,3-dielectrophilic properties have now been examined successfully in this work. They are shown to react with ethyl thioglycolate in the
Synthesis, cytotoxicity and effects of some 1,2,4-triazole and 1,3,4-thiadiazole derivatives on immunocompetent cells
Mavrova, Anelia Ts.,Wesselinova, Diana,Tsenov, Yordan A.,Denkova, Pavletta
experimental part, p. 63 - 69 (2009/04/07)
Novel derivatives of 4,5-substituted-1,2,4-triazole-thiones and 2,5-substituted-1,3,4-thiadiazoles were synthesized and evaluated for their cytotoxicity. The biological study indicated that compounds 4-ethyl-5-(4,5,6,7-tetrahydro-1-benzothien-2-yl)-2,4-di
