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2-AMINO-5-TERT-BUTYL-BENZOIC ACID is a chemical compound with the molecular formula C13H17NO2, belonging to the benzoic acid derivatives. It features an amino group and a tert-butyl group, which contribute to its unique structure and properties. 2-AMINO-5-TERT-BUTYL-BENZOIC ACID holds potential in pharmaceuticals and organic synthesis, making it a valuable asset for research and development in chemistry and pharmaceuticals.

2475-77-6

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2475-77-6 Usage

Uses

Used in Pharmaceutical Industry:
2-AMINO-5-TERT-BUTYL-BENZOIC ACID is used as an active pharmaceutical ingredient for the development of new drugs. Its unique structure and functional groups allow it to be a promising candidate for treating various medical conditions.
Used in Organic Synthesis:
2-AMINO-5-TERT-BUTYL-BENZOIC ACID is used as a building block in organic synthesis for the creation of complex organic molecules. Its versatile structure makes it suitable for the synthesis of a wide range of compounds.
Used as a Starting Material:
2-AMINO-5-TERT-BUTYL-BENZOIC ACID is used as a starting material for the synthesis of other compounds. Its presence in the initial stages of a chemical reaction can lead to the formation of various products with different applications.
Used as a Reagent:
2-AMINO-5-TERT-BUTYL-BENZOIC ACID is used as a reagent in various chemical reactions. Its functional groups can participate in multiple types of reactions, making it a useful component in the synthesis process.

Check Digit Verification of cas no

The CAS Registry Mumber 2475-77-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,7 and 5 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2475-77:
(6*2)+(5*4)+(4*7)+(3*5)+(2*7)+(1*7)=96
96 % 10 = 6
So 2475-77-6 is a valid CAS Registry Number.
InChI:InChI=1/C11H15NO2/c1-11(2,3)7-4-5-9(12)8(6-7)10(13)14/h4-6H,12H2,1-3H3,(H,13,14)

2475-77-6Relevant academic research and scientific papers

Oxidative fluorination of N-arylsulfonamides

Buckingham, Faye,Calderwood, Samuel,Checa, Bego?a,Keller, Thomas,Tredwell, Matthew,Collier, Thomas Lee,Newington, Ian M.,Bhalla, Rajiv,Glaser, Matthias,Gouverneur, Véronique

supporting information, p. 33 - 39 (2015/09/22)

We report a late stage oxidative nucleophilic fluorination of N-arylsulfonamides, a class of compounds so far not considered as precursors to 4-fluorophenyl sulfonamides. By installing a para-positioned tert-butyl substituent on the aniline, oxidative fluorination takes place regioselectively in the presence of HF·pyridine and PIDA. This methodology has been shown to give good yields for a variety of ortho- and meta-functionalised N-arylsulfonamides and has been adapted for radiofluorination to give 4-[18F]fluorophenyl sulfonamides under carrier added conditions.

Anti-inflammatory oxazole[4,5-b]pyridines

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, (2008/06/13)

The various isomers of oxazolo- and thiazolopyridines having utility as antiinflammatory, antipyretic and analgesic agents are prepared by condensation of an appropriate amino-hydroxypyridine or amino-mercaptopyridine with a carboxylic acid, halide or anhydride.

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