53982-01-7

Basic information

• Product Name: Benzenamine, 2-ethyl-6-methoxy-
• Synonyms: Benzenamine,2-ethyl-6-methoxy;2-methoxy-6-ethylaniline
• CAS NO: 53982-01-7
• Molecular Formula: C9H13NO
• Molecular Weight: 151.208
• Mol File: 53982-01-7.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: Benzenamine, 2-ethyl-6-methoxy-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenamine, 2-ethyl-6-methoxy-(53982-01-7)
• EPA Substance Registry System: Benzenamine, 2-ethyl-6-methoxy-(53982-01-7)

Safety Data

• Hazardous Substances Data: 53982-01-7(Hazardous Substances Data)

Upstream product

• 66107-33-3 3-methoxyphenyl triflate 
• 150-19-6 O-methylresorcine 
• 398136-31-7 tert-butyl 2-ethyl-6-methoxyphenylcarbamate 
• 33852-43-6 1-(3-methoxy-2-nitrophenyl)ethanone 
• 16029-98-4 trimethylsilyl iodide 
• 195529-68-1 2-Nitro-3-(1-hydroxyethyl)anisole 
• 150330-40-8 2-Methoxy-6-vinyl-1-nitrobenzene 
• 53055-05-3 3-methoxy 2-nitrobenzaldehyde 
• 154150-18-2 tert-butyl 2-methoxyphenylcarbamate 
• 90-04-0 2-methoxy-phenylamine 

Downstream Products

• 1027924-09-9 1-(2-Ethyl-6-methoxy-phenyl)-3-pentyl-urea 
• 148726-45-8 1-(2-Ethyl-6-hydroxy-phenyl)-3-pentyl-urea 
• 398136-39-5 2-amino-3-ethylphenol 
• 53981-77-4 2-Chloro-N-(2-ethyl-6-methoxy-phenyl)-N-(2-methoxy-1-methyl-ethyl)-acetamide 
• 53981-76-3 2-Chloro-N-(2-ethyl-6-methoxy-phenyl)-N-(2-methoxy-ethyl)-acetamide 

Relevant articles and documents

ortho-Difunctionalization of arynes by LiZnEt2(TMP)-mediated deprotonative zincation/elimination of aryl triflates

Generation of arynes from aryl triflates has been achieved using lithium diethyl(tetramethylpiperidyl)-zincate base LiZnEt2(TMP), via a directed ortho-deprotonative zincation and subsequent elimination of the triflate group. The aryne formation

5-[3-[PIPERIDIN-1-YL]-3-OXO-PROPYL]-IMIDAZOLIDINE-2,4-DIONE DERIVATIVES AS ADAMTS 4 AND 5 INHIBITORS FOR TREATING E.G. OSTEOARTHRITIS

The present invention discloses 5-[3-[piperazin-l-yl]-3-oxo-propyl]-imidazolidine-2,4-dione derivatives according to Formula (I), wherein R1, R2, R3a, R3b, R6a, R6b, the subscript n and Cy are as defined herein. The present invention relates to compounds inhibiting ADAMTS 4 and 5 for the prophylaxis or treatment of inflammatory diseases or diseases involving degradation of cartilage or disruption of cartilage homeostasis, such as e.g. osteoarthritis.

Chiral relay effect: 4-substituted 1,3-benzoxazol-2-(3H)-ones as achiral templates for enantioselective Diels-Alder reactions

(matrix presented) A new strategy to control the enantioselectivity of Lewis acid catalyzed reactions has been investigated. The use of N-acryloyl-1,3-benzoxazol-2-(3H)-ones substituted at position 4 leads to the formation of diastereomeric complexes as a