97271-97-1 Usage
Description
2-AMINO-3-NITRO-BENZALDEHYDE is an aromatic aldehyde chemical compound with the molecular formula C7H6N2O3. It features a benzene ring with a nitro and amino group attached, known for its bright yellow color and versatile applications in various industries.
Uses
Used in Organic Synthesis:
2-AMINO-3-NITRO-BENZALDEHYDE is used as an intermediate in organic synthesis for the production of pharmaceuticals, dyes, and other organic compounds. Its unique structure allows for the creation of a wide range of derivatives with diverse properties and applications.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-AMINO-3-NITRO-BENZALDEHYDE is used as a key intermediate in the synthesis of various drugs. Its potential pharmacological properties, such as antibacterial and antifungal activities, make it a valuable compound for the development of new medications.
Used in Dye Industry:
2-AMINO-3-NITRO-BENZALDEHYDE is used as a dye in the dye industry due to its bright yellow color. It is employed in various applications, including textiles, plastics, and other materials, to impart color and enhance visual appeal.
Used in Research and Development:
2-AMINO-3-NITRO-BENZALDEHYDE is also used in research and development for studying its potential applications and properties. Its unique structure and reactivity make it an interesting subject for scientific investigations, leading to new discoveries and innovations in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 97271-97-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,2,7 and 1 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 97271-97:
(7*9)+(6*7)+(5*2)+(4*7)+(3*1)+(2*9)+(1*7)=171
171 % 10 = 1
So 97271-97-1 is a valid CAS Registry Number.
97271-97-1Relevant articles and documents
Chiral Phosphoric-Acid-Catalyzed Cascade Prins Cyclization
Sun, Huai-Ri,Zhao, Qingyang,Yang, Hui,Yang, Sen,Gou, Bo-Bo,Chen, Jie,Zhou, Ling
supporting information, p. 7143 - 7148 (2019/09/07)
Asymmetric Prins cyclization of in situ generated quinone methides and o-aminobenzaldehyde has been developed with chiral phosphoric acid as an efficient catalyst. This unconventional method provides a facile access to diverse functionalized trans-fused pyrano-/furo-tetrahydroquinoline derivatives in excellent yield and with excellent diastereo- and enantioselectivities (up to 99% yield and 99% ee). Mechanistic studies suggested that the three adjacent tertiary stereocenters were constructed through the sequential formation of C-O, C-C, and C-N bonds.
OXIDATIVE DEGRADATION OF 8-NITROQUINOLINE WITH HYDROGEN PEROXIDE IN ACETIC ACID --- A POSSIBLE MECHANISM THROUGH 3,4-EPOXIDE OF QUINOLINE RING
Kaiya, Toyo,Kawazoe, Yutaka
, p. 511 - 518 (2007/10/02)
The treatment of 8-nitroquinoline with hydrogen peroxide and acetic acid at 60 grad C afforded 7-nitroindole, 7-nitro-2-oxindole, 2-amino-3-nitrobenzoic acid, 2-amino-3-nitrobenzaldehyde, 3,4-dihydro-3,4-trans-dihydroxy-8-nitrocarbostyril, 3,4-trans-dihyd
