17332-54-6 Usage
Derivative of benzoic acid
Benzoic acid derivative This compound is derived from benzoic acid, which means it has a similar structure with modifications in its functional groups.
Tert-butyl-phenylamino group
Unique functional group The presence of a tert-butyl-phenylamino group gives this compound its unique chemical properties and potential applications in various fields.
Use as a reagent
Organic synthesis and pharmaceutical research 2-(3-tert-butyl-phenylamino)-benzoic acid is often used as a reagent in organic synthesis and pharmaceutical research, aiding in the development of new compounds and drugs.
Potential applications
New drug development and pharmaceuticals Due to its unique chemical properties, this compound has potential applications in the development of new drugs and pharmaceuticals.
Industrial uses
Polymer and material production 2-(3-tert-butyl-phenylamino)-benzoic acid may also have industrial applications in the production of polymers and other materials.
Fields of potential
Pharmaceuticals, materials science, and chemical research This chemical compound has potential in various fields, including pharmaceuticals, materials science, and chemical research, due to its unique properties and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 17332-54-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,3,3 and 2 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 17332-54:
(7*1)+(6*7)+(5*3)+(4*3)+(3*2)+(2*5)+(1*4)=96
96 % 10 = 6
So 17332-54-6 is a valid CAS Registry Number.
InChI:InChI=1/C17H19NO2/c1-17(2,3)12-7-6-8-13(11-12)18-15-10-5-4-9-14(15)16(19)20/h4-11,18H,1-3H3,(H,19,20)
17332-54-6Relevant articles and documents
An enantioselective fluorescence sensing assay for quantitative analysis of chiral carboxylic acids and amino acid derivatives
Wolf, Christian,Liu, Shuanglong,Reinhardt, Brian C.
, p. 4242 - 4244 (2006)
A chiral 1,8-diacridylnaphthalene-derived fluorosensor exhibiting a C 2-symmetric cleft designed for stereoselective interactions with hydrogen bond donors has been used for the determination of both concentration and enantiomeric composition of carboxylic acids and amino acid derivatives. The Royal Society of Chemistry 2006.
Regioselective copper-catalyzed amination of chlorobenzoic acids: Synthesis and solid-state structures of N-aryl anthranilic acid derivatives
Mei, Xuefeng,August, Adam T.,Wolf, Christian
, p. 142 - 149 (2007/10/03)
A chemo- and regioselective copper-catalyzed cross-coupling reaction for effective amination of 2-chlorobenzoic acids with aniline derivatives has been developed. The method eliminates the need for acid protection and produces a wide range of N-aryl anthranilic acid derivatives in up to 99% yield. The amination was found to proceed with both electron-rich and electron-deficient aryl chlorides and anilines and also utilizes sterically hindered anilines such as 2,6-dimethylaniline and 2-tert-butylaniline. The conformational isomerism of appropriately substituted N-aryl anthranilic acids has been investigated in the solid state. Crystallographic analysis of seven anthranilic acid derivatives showed formation of two distinct supramolecular architectures exhibiting trans-anti and unprecedented trans-syn dimeric structures.
