74103-28-9 Usage
Description
4-(acetylamino)-3-bromobenzoic acid is an aromatic carboxylic acid derivative with the molecular formula C9H8BrNO3. It features a benzene ring with a bromine atom and an acetylamino group attached, providing unique structural and reactive properties.
Used in Pharmaceutical Industry:
4-(acetylamino)-3-bromobenzoic acid is used as a key intermediate in the synthesis of pharmaceuticals for its potential role in drug discovery and development. Its unique structure allows for the creation of complex molecules with specific therapeutic properties.
Used in Fine Chemicals Production:
In the fine chemicals industry, 4-(acetylamino)-3-bromobenzoic acid serves as a valuable building block in organic synthesis. It contributes to the production of specialty chemicals with tailored properties for various applications.
Used in Organic Synthesis:
4-(acetylamino)-3-bromobenzoic acid is utilized as a starting material in organic synthesis to construct more complex molecules. Its reactivity and structural features enable the development of compounds with specific functions, further expanding its industrial and scientific significance.
Check Digit Verification of cas no
The CAS Registry Mumber 74103-28-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,1,0 and 3 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 74103-28:
(7*7)+(6*4)+(5*1)+(4*0)+(3*3)+(2*2)+(1*8)=99
99 % 10 = 9
So 74103-28-9 is a valid CAS Registry Number.
74103-28-9Relevant articles and documents
Bromodecarbonylation and bromodecarboxylation of electron-rich benzaldehydes and benzoic acids with oxone and sodium bromide
Koo, Bon-Suk,Kim, Eun-Hoo,Lee, Kee-Jung
, p. 2275 - 2286 (2007/10/03)
Benzaldehydes and benzoic acids bearing ortho- and paraelectron donating substituents having unshared electron-pair have undergone bromodecarbonylation or bromodecarboxylation on treatment with sodium bromide in the presence of Oxone in aqueous methanol.
