1208233-15-1

Basic information

• Product Name: tert-butyl (2E)-3-[3-(3-methylbut-2-en-1-yl)-4-[(3-phenylpropanoyl)oxy]phenyl]prop-2-enoate
• Synonyms: tert-butyl (2E)-3-[3-(3-methylbut-2-en-1-yl)-4-[(3-phenylpropanoyl)oxy]phenyl]prop-2-enoate
• CAS NO: 1208233-15-1
• Molecular Weight: 420.549
• Mol File: 1208233-15-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: tert-butyl (2E)-3-[3-(3-methylbut-2-en-1-yl)-4-[(3-phenylpropanoyl)oxy]phenyl]prop-2-enoate(CAS DataBase Reference)
• NIST Chemistry Reference: tert-butyl (2E)-3-[3-(3-methylbut-2-en-1-yl)-4-[(3-phenylpropanoyl)oxy]phenyl]prop-2-enoate(1208233-15-1)
• EPA Substance Registry System: tert-butyl (2E)-3-[3-(3-methylbut-2-en-1-yl)-4-[(3-phenylpropanoyl)oxy]phenyl]prop-2-enoate(1208233-15-1)

Safety Data

• Hazardous Substances Data: 1208233-15-1(Hazardous Substances Data)

Upstream product

• 870-63-3 prenyl bromide 
• 540-38-5 p-Iodophenol 
• 151071-03-3 4-iodo-2-(3-methylbut-2-en-1-yl)phenol 
• 1663-39-4 tert-Butyl acrylate 
• 1208233-13-9 4-iodo-2-(3-methylbut-2-en-1-yl)phenyl-3-phenylpropanoate 

Relevant articles and documents

Potent and Highly Selective Aldo-Keto Reductase 1C3 (AKR1C3) Inhibitors Act as Chemotherapeutic Potentiators in Acute Myeloid Leukemia and T-Cell Acute Lymphoblastic Leukemia

Aldo-keto reductase 1C3 (AKR1C3) catalyzes the synthesis of 9α,11β-prostaglandin (PG) F2α and PGF2α prostanoids that sustain the growth of myeloid precursors in the bone marrow. The enzyme is overexpressed in acute myeloid leukemia (

Inhibitory activity of Brazilian green propolis components and their derivatives on the release of cys-leukotrienes

The effects of Brazilian green propolis ethanol extract on Cry j1-induced cys-leukotrienes and histamine release from peripheral leukocytes of patients with allergic rhinitis were investigated. One of the key mechanisms for the anti-allergic properties of the extract was revealed to be the suppression of cys-LTs release. Furthermore, a series of propolis components and their phenethyl esters were synthesized and evaluated as inhibitors of cys-LTs release. Artepillin C, baccharin, and kaempferide were the major active components of the ethanol extract. The inhibitory activity of artepillin C phenethyl ester was comparable to that of existing LT synthesis inhibitors. Crown Copyright