398136-31-7

Basic information

• Product Name: TERT-BUTYL 2-ETHYL-6-METHOXYPHENYLCARBAMATE
• Synonyms: TERT-BUTYL 2-ETHYL-6-METHOXYPHENYLCARBAMATE
• CAS NO: 398136-31-7
• Molecular Formula: C₁₄H₂₁NO₃
• Molecular Weight: 251.32
• Mol File: 398136-31-7.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: TERT-BUTYL 2-ETHYL-6-METHOXYPHENYLCARBAMATE(CAS DataBase Reference)
• NIST Chemistry Reference: TERT-BUTYL 2-ETHYL-6-METHOXYPHENYLCARBAMATE(398136-31-7)
• EPA Substance Registry System: TERT-BUTYL 2-ETHYL-6-METHOXYPHENYLCARBAMATE(398136-31-7)

Safety Data

• Hazardous Substances Data: 398136-31-7(Hazardous Substances Data)

Upstream product

• 90-04-0 2-methoxy-phenylamine 
• 24424-99-5 di-tert-butyl dicarbonate 
• 75-03-6 ethyl iodide 
• 154150-18-2 tert-butyl 2-methoxyphenylcarbamate 

Downstream Products

• 53982-01-7 2-Ethyl-6-methoxyaniline 
• 398136-39-5 2-amino-3-ethylphenol 

Relevant articles and documents

5-[3-[PIPERAZIN-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