31539-91-0

Basic information

• Product Name: N-(2-ISOPROPYL-4-NITROPHENYL)ACETAMIDE
• Synonyms: N-(2-ISOPROPYL-4-NITROPHENYL)ACETAMIDE
• CAS NO: 31539-91-0
• Molecular Formula: C₁₁H₁₄N₂O₃
• Molecular Weight: 222.24
• Mol File: 31539-91-0.mol

Chemical Properties

• Boiling Point: 391.2±42.0 °C(Predicted)
• Appearance: /
• Density: 1.205±0.06 g/cm3(Predicted)
• PKA: 13.88±0.70(Predicted)
• CAS DataBase Reference: N-(2-ISOPROPYL-4-NITROPHENYL)ACETAMIDE(CAS DataBase Reference)
• NIST Chemistry Reference: N-(2-ISOPROPYL-4-NITROPHENYL)ACETAMIDE(31539-91-0)
• EPA Substance Registry System: N-(2-ISOPROPYL-4-NITROPHENYL)ACETAMIDE(31539-91-0)

Safety Data

• Hazardous Substances Data: 31539-91-0(Hazardous Substances Data)

Upstream product

• 108-24-7 acetic anhydride 
• 643-28-7 2-isopropylaniline 
• 19246-04-9 N-(2-isopropylphenyl)acetamide 

Downstream Products

• 857539-14-1 2-isopropyl-4-nitro-benzoic acid 
• 60515-72-2 4‐nitro‐2‐(propan‐2‐yl)phenol 
• 1029803-93-7 2-isopropyl-4-nitrobenzoic acid 2-(2-isopropylimidazol-1-yl)ethyl ester 
• 1029803-73-3 2-isopropyl-4-nitrobenzoic acid 2-bromoethyl ester 
• 1029803-71-1 2-isopropyl-4-nitrobenzonitrile 
• 31539-92-1 2-iodo-5-nitroisopropylbenzene 

Relevant articles and documents

2- [ (2-SUBSTITUTED) -IND0LIZIN-3-YL] -2-OXO-ACETAMIDE DERIVATIVES AS ANTIFUNGAL AGENTS

The invention provides compounds of formula (I), and pharmaceutically acceptable salts thereof wherein: Rl, R2, R3, R4, R5, R6, R7, X and X1 are as defined herein. These compounds are useful in the manufacture of medicaments for use in the prevention or treatment of a fungal disease. Compounds of formula (I), and agriculturally acceptable salts thereof, may also be used as agricultural fungicides.

Substituted 2-arylimino heterocycles and compositions containing them, for use as progesterone receptor binding agents

This invention relates to 2-arylimino heterocycles, including 2-arylimino-1,3-thiazolidines, 2-arylimino-2,3,4,5-tetrahydro-1,3-thiazines, 2-arylimino-1,3-thiazolidin-4-ones, 2-arylimino-1,3-thiazolidin-5-ones, and 2-arylimino-1,3-oxazolidines, and their use in modulating progesterone receptor mediated processes, and pharmaceutical compositions for use in such therapies.

Hydroxylamine derivative of 5-nitro-8-hydroxy quinoline

Novel hydroxylamino derivatives of the formula wherein Ar is selected from the group consisting of mono- and polycyclic aromatics and hetero-aromatics, both optionally substituted with at least one member of the group consisting of --OH, halogen, --NO2, --CN, STR1 --R7, --OR8, STR2 --SO2 R12, --SO3 R13, --COOR14, aryl of 6 to 14 carbon atoms, --OR16, --CH2 --CN and --CH2 SO2 --R15, R1, R2, R3, R4, R5 and R6 are individually selected from the group consisting of hydrogen and alkyl of 1 to 8 carbon atoms, R7 and R8 are optionally unsaturated alkyl of 1 to 8 carbon atoms optionally substituted with at least one member of the group consisting of halogen and cyano, R9, R10, R11, R12 and R13 are alkyl of 1 to 8 carbon atoms, Z is selected from the group consisting of hydrogen, optionally unsaturated alkyl of 1 to 8 carbon atoms and acyl of an organic carboxylic acid of 2 to 18 carbon atoms, R14 is selected from the group consisting of hydrogen and alkyl of 1 to 8 carbon atoms, R15 is selected from the group consisting of alkyl of 1 to 8 carbon atoms and aryl of 6 to 14 carbon atoms optionally substituted with an alkyl of 1 to 8 carbon atoms, R16 is aryl of 6 to 14 carbon atoms optionally substituted with a member of the group consisting of alkyl of 1 to 8 carbon atoms, halogen and --NO2, the substituents of Ar being able to form rings containing at least one heteroatom selected from the group consisting of oxygen, nitrogen and sulfur and their non-toxic agriculturally acceptable acid addition salts with the proviso Ar is not phenyl nor phenyl with one methyl in the 2,3 or 4 position, a nitro in the 2- or 4-position, a chlorine in the 3- or 4-position, a bromine in the 4-position or a --CF3 in the 4-position nor 2,4-dinitrophenyl nor 2-nitro-4-trifluoromethylphenyl nor 2,6-dinitrophenyl nor 2,4,6-trinitrophenyl nor 2,4-dinitro-6-trifluoromethylphenyl useful for increasing vegetation growth and increasing crop yields and their preparation.