159435-03-7 Usage
Description
4-DIMETHYLAMINO-2-HYDROXY-2'-METHOXYCARBONYL-4'-NITROBENZOPHENONE is a synthetic intermediate with a complex chemical structure. It is characterized by its unique arrangement of functional groups, including a dimethylamino, hydroxy, methoxycarbonyl, and nitro groups attached to a benzophenone core. 4-DIMETHYLAMINO-2-HYDROXY-2'-METHOXYCARBONYL-4'-NITROBENZOPHENONE is known for its potential applications in various chemical and pharmaceutical processes due to its versatile chemical properties.
Uses
Used in Chemical Synthesis:
4-DIMETHYLAMINO-2-HYDROXY-2'-METHOXYCARBONYL-4'-NITROBENZOPHENONE is used as a synthetic intermediate for the preparation of various complex organic compounds. Its unique structure allows it to serve as a building block in the synthesis of a wide range of molecules, including pharmaceuticals, dyes, and other specialty chemicals.
Used in Fluorescent Labeling:
4-DIMETHYLAMINO-2-HYDROXY-2'-METHOXYCARBONYL-4'-NITROBENZOPHENONE is used as an intermediate for the preparation of rhodamine derivatives, which are widely used as fluorescent labels in various scientific applications. These labels are valuable tools in fields such as biochemistry, molecular biology, and cell biology, where they are used for the detection, visualization, and tracking of specific molecules or cellular structures.
Check Digit Verification of cas no
The CAS Registry Mumber 159435-03-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,9,4,3 and 5 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 159435-03:
(8*1)+(7*5)+(6*9)+(5*4)+(4*3)+(3*5)+(2*0)+(1*3)=147
147 % 10 = 7
So 159435-03-7 is a valid CAS Registry Number.
159435-03-7Relevant articles and documents
Synthesis and Characterisation of Pure Isomers of Iodoacetamidotetramethylrhodamine
Corrie, John E. T.,Craik, James S.
, p. 2967 - 2974 (2007/10/02)
The isomeric benzoylnitrobenzoate esters 5 and 6, prepared by condensation of 4-nitrophthalic anhydride and 3-(dimethylamino)phenol followed by esterification, were separated by fractional crystallisation and their structures assigned by NOE difference spectroscopy.Reduction of the nitro group in each compound followed by acetylation and ester hydrolysis gave the isomeric acetamido acids 7 and 8, which were efficiently condensed with 3-(diemthylamino)phenol in the presence of trimethylsilyl polyphosphate to give the acetamidorhodamines 9 and 10, respectively.These compounds were converted by standard means into the pure 6- and 5-(iodoacetamido)tetramethylrhodamines 1 and 2.The visible spectroscopic properties of the compounds were examined and accurate extinction determined.