144583-89-1

Basic information

• Product Name: 1,4,4-Trimethyl-6-nitro-3,4-dihydro-1H-quinolin-2-one
• Synonyms: 1,4,4-Trimethyl-6-nitro-3,4-dihydro-1H-quinolin-2-one;1,4,4-Trimethyl-6-nitro-3,4-dihydroquinolin-2(1H)-one;3,4-Dihydro-1,4,4-trimethyl-6-nitroquinolin-2(1H)-one;1,4,4-TRIMETHYL-6-NITRO-3H-QUINOLIN-2-ONE
• CAS NO: 144583-89-1
• Molecular Formula: C12H14N2O3
• Molecular Weight: 234.25116
• Mol File: 144583-89-1.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1,4,4-Trimethyl-6-nitro-3,4-dihydro-1H-quinolin-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: 1,4,4-Trimethyl-6-nitro-3,4-dihydro-1H-quinolin-2-one(144583-89-1)
• EPA Substance Registry System: 1,4,4-Trimethyl-6-nitro-3,4-dihydro-1H-quinolin-2-one(144583-89-1)

Safety Data

• Hazardous Substances Data: 144583-89-1(Hazardous Substances Data)

Usage

Uses

Used in Fluorescent Dyes and Pigments Production:
1,4,4-Trimethyl-6-nitro-3,4-dihydro-1H-quinolin-2-one is used as a key component in the production of fluorescent dyes and pigments, providing unique optical properties and color characteristics.
Used in Pharmaceuticals and Research Chemicals:
1,4,4-Trimethyl-6-nitro-3,4-dihydro-1H-quinolin-2-one is used as a component in pharmaceuticals and research chemicals, contributing to the development of new drugs and chemical compounds.
It is important to handle 1,4,4-Trimethyl-6-nitro-3,4-dihydro-1H-quinolin-2-one with care, as it is toxic if ingested or inhaled, and can cause irritation to the skin and eyes upon contact.

Upstream product

• 20886-48-0 1,4,4-trimethyl-3,4-dihydroquinolin-2(1H)-one 

Downstream Products

• 144583-88-0 6-amino-1,4,4-trimethyl-3,4-dihydroquinolin-2(1H)-one 

Relevant articles and documents

Synthesis of potential Rho-kinase inhibitors based on the chemistry of an original heterocycle: 4,4-Dimethyl-3,4-dihydro-1H-quinolin-2-one

A new series of substituted 4,4-dimethyl-3,4-dihydro-1H-quinolin-2-one have been prepared via condensation of 3,3-dimethylacryloyl chloride with aniline. Details of synthetic procedures are shown. Our aim was to investigate the potency of our original het

Carboxamides and anilides

Described herein are compounds of the formula STR1 wherein R1 signifies hydrogen, lower-alkyl or a cation; R2 signifies hydrogen, lower-alkyl, lower-alkoxy or halogen; M signifies --CONH-- or --NHCO--; X and Y are each independently selected from the group consisting of >CR3 R4 and --CONR5 --; Z signifies >CR6 R7 ; R3, R4, R6 and R7 are each independently selected from the group consisting of hydrogen and lower-alkyl; R5 signifies alkyl; and n signifies 0, 1 or 2; provided that at least one of X or Y is --CONR5 -- which is bonded to the phenyl ring via the N atom. These compounds are useful in the treatment and prophylaxis of neoplasms, dermatoses and aging of the skin.