2122-63-6 Usage
Description
4-AMINO-3-IODOBENZOIC ACID is an organic compound that serves as a key building block in the synthesis of various pharmaceuticals and chemical compounds. It features an aromatic ring with an amino group at the 4-position and an iodine atom at the 3-position, which can be further functionalized to create a wide range of derivatives.
Uses
Used in Pharmaceutical Industry:
4-AMINO-3-IODOBENZOIC ACID is used as a synthetic intermediate for the development of various drugs and pharmaceutical agents. Its unique structure allows for the attachment of different functional groups, making it a versatile component in the synthesis of new compounds with potential therapeutic applications.
Used in Chemical Research:
In the field of chemical research, 4-AMINO-3-IODOBENZOIC ACID is utilized as a starting material for the preparation of novel organic compounds and materials. Its reactivity and structural features enable the exploration of new chemical reactions and the discovery of innovative applications.
Used in Resin-bound Compounds:
4-AMINO-3-IODOBENZOIC ACID is used in the generation of resin-bound compounds, such as 3-[2-(acetylamino)ethyl]-2-iodo-1H-indole-5-carboxamide, which are synthesized starting from Polystyrene-Rink resin. These resin-bound compounds have potential applications in various fields, including drug discovery and chemical synthesis.
Check Digit Verification of cas no
The CAS Registry Mumber 2122-63-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,2 and 2 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2122-63:
(6*2)+(5*1)+(4*2)+(3*2)+(2*6)+(1*3)=46
46 % 10 = 6
So 2122-63-6 is a valid CAS Registry Number.
InChI:InChI=1/C7H6INO2/c8-5-3-4(7(10)11)1-2-6(5)9/h1-3H,9H2,(H,10,11)
2122-63-6Relevant articles and documents
Solid-phase synthesis of heterocycles via palladium-catalyzed annulation
Wang, Yao,Huang, Tai-Nang
, p. 9605 - 9608 (1998)
Solid-phase linked o-iodoanilines (4) and o-iodophenol (9) reacted with 1,3- and 1,4-dienes in the presence of palladium acetate to generate highly substituted indolines, tetrahydroquinolines, hydrobenzofurans and hydrobenzopyrans, which provided an effic
Spin system assignment of homo-o-phenylene ethynylene oligomers
Slutsky, Morris M.,Jones, Ticora V.,Tew, Gregory N.
, p. 342 - 347 (2007)
We previously reported the synthesis and solution characterization of short o-phenylene ethynylene (oPE) foldamers. Proton correlation techniques are not adequate for NMR assignment in these compounds as the ethynylene linkers interrupt proton connectivit
Heteroaryl carboxamides
-
Page/Page column 11, (2015/11/16)
The invention relates to novel heteroaryl carboxamides, a process for their preparation, and pharmaceutical compositions containing them. These materials are useful for the treatment and/or prophylaxis of diseases and for improving perception, concentrati
Ground-state elevation approach to suppress side reactions in gold-sensing systems based on alkyne activation
Seo, Hyewon,Jun, Mi Eun,Ranganathan, Koteeswari,Lee, Kyung-Ha,Kim, Kyong-Tai,Lim, Woocherl,Rhee, Young Min,Ahn, Kyo Han
supporting information, p. 1374 - 1377 (2014/04/03)
A novel approach to suppress the side reactions observed in the reaction-based gold-sensing systems based on the alkyne activation is disclosed. By elevating steric strain around the reaction site, the gold ion promoted ring-opening process in rhodamine-l
