103554-42-3 Usage
Derivative of benzoic acid
It is a modified version of benzoic acid This means that the compound is structurally related to benzoic acid, with some modifications in its chemical structure.
Contains a tert-butyl group
The presence of a tert-butyl group (C4H9) This is a specific type of alkyl group that is part of the compound's structure.
Contains a phenylamino group
The presence of a phenylamino group (C6H5NH2) This is another specific functional group in the compound's structure.
Used in the pharmaceutical industry
As an intermediate in the synthesis of various medications and dyes This indicates that the compound plays a role in the production of other pharmaceuticals and dyes.
Exhibits anti-inflammatory and analgesic properties
It has the potential to reduce inflammation and relieve pain This suggests that the compound may be useful in the development of new therapeutic drugs for pain and inflammation.
Important building block in the production of various pharmaceutical and cosmetic products
It is a key component in the synthesis of other compounds This highlights the compound's significance in the creation of a wide range of products in the pharmaceutical and cosmetic industries.
Check Digit Verification of cas no
The CAS Registry Mumber 103554-42-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,5,5 and 4 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 103554-42:
(8*1)+(7*0)+(6*3)+(5*5)+(4*5)+(3*4)+(2*4)+(1*2)=93
93 % 10 = 3
So 103554-42-3 is a valid CAS Registry Number.
InChI:InChI=1/C17H19NO2/c1-17(2,3)13-9-5-7-11-15(13)18-14-10-6-4-8-12(14)16(19)20/h4-11,18H,1-3H3,(H,19,20)
103554-42-3Relevant articles and documents
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 (2006)
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.
