142141-38-6

Basic information

• Product Name: Benzamide, 2-amino-3-methyl-N-propyl-
• CAS NO: 142141-38-6
• Molecular Formula: C11H16N2O
• Molecular Weight: 192.261
• Mol File: 142141-38-6.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: Benzamide, 2-amino-3-methyl-N-propyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzamide, 2-amino-3-methyl-N-propyl-(142141-38-6)
• EPA Substance Registry System: Benzamide, 2-amino-3-methyl-N-propyl-(142141-38-6)

Safety Data

• Hazardous Substances Data: 142141-38-6(Hazardous Substances Data)

Upstream product

• 107-10-8 propylamine 
• 4389-45-1 3-methylantranilic acid 
• 95-53-4 o-toluidine 
• 1132-03-2 2-(hydroxyimino)-N-(2-methylphenyl)acetamide 
• 1127-59-9 7-methyl-1H-indole-2,3-dione 
• 1397833-51-0 (2-amino-3-methylphenyl) (benzotriazole-1-yl)methanone 

Downstream Products

• 142141-43-3 2-Methyl-6-propylaminomethyl-phenylamine 
• 1217506-24-5 C₂₂H₂₁ClF₃N₅O₃ 
• 1217506-79-0 3-(allyloxy)-1-(3-chloropyridin-2-yl)-N-(2-methyl-6-(propylcarbamoyl)phenyl)-1H-pyrazole-5-carboxamide 
• 1447721-15-4 C₂₁H₂₀BrClN₆O₂S 
• 1392234-85-3 C₂₂H₂₀ClF₃N₆O₃ 
• 1257070-00-0 C₂₃H₂₄ClN₅O₄ 
• 1257069-43-4 C₂₃H₂₄ClN₅O₄ 

Relevant articles and documents

Diversification of quinazolinones by Pd-catalyzed C(sp3)-acetoxylation

The quinazolinone ring has been exploited as a directing group for C(sp3)-H functionalization for the first time. The proximal C-γ(sp3)-H bonds have been oxidized by palladium-catalyzed acetoxylation reaction. Various functional grou

Synthesis, crystal structure and biological activity of a novel anthranilic diamide insecticide containing allyl ether

In search of environmentally benign insecticides with high activity, low toxicity and low residue, a series of novel anthranilic diamides containing allyl ether were designed and synthesized. All the compounds were characterized by 1H NMR spectroscopy, HRMS or elemental analysis. The single crystal structure of 18e was determined by X-ray diffraction. The insecticidal activities of the new compounds were evaluated. The results showed that some compounds exhibited excellent insecticidal activities against Lepidoptera pests. Among this series compounds, 18l showed 100 % larvicidal activity against Mythimna separate Walker and Plutella xylostella Linnaeus at the test concentration.

A new protocol for the synthesis of primary, secondary and tertiary anthranilamides utilizing N-(2-aminoarylacyl)benzotriazoles

A convenient route for efficient conversion of unprotected anthranilic acids into the corresponding N-(2-aminoarylacyl)benzotrazoles is described. N-(2-Aminoarylacyl)-benzotrazoles have been successfully used to synthesize primary, secondary and tertiary anthranilamides in high yields (71-96%). ARKAT-USA, Inc.