15424-04-1

Basic information

• Product Name: 3-(2-BROMO-ETHOXY)-PROPENE
• Synonyms: 3-(2-BROMO-ETHOXY)-PROPENE;2-Allyloxyethyl bromide
• CAS NO: 15424-04-1
• Molecular Formula: C₅H₉BrO
• Molecular Weight: 165.03
• Mol File: 15424-04-1.mol

Chemical Properties

• Boiling Point: 68.5-69 °C(Press: 36 Torr)
• Appearance: /
• Density: 1.336 g/cm3
• CAS DataBase Reference: 3-(2-BROMO-ETHOXY)-PROPENE(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(2-BROMO-ETHOXY)-PROPENE(15424-04-1)
• EPA Substance Registry System: 3-(2-BROMO-ETHOXY)-PROPENE(15424-04-1)

Safety Data

• Hazardous Substances Data: 15424-04-1(Hazardous Substances Data)

Upstream product

• 111-45-5 ethylene glycol monoallyl ether 
• 75-21-8 oxirane 
• 106-95-6 allyl bromide 
• 107-21-1 ethylene glycol 
• 50563-72-9 2-(allyloxy)ethyl 4-methylbenzenesulfonate 

Downstream Products

• 3917-15-5 allyl vinyl ether 
• 124391-75-9 3-tetrahydrofuranmethanol 
• 156418-97-2 6-Oxa-8-nonene-2-one 
• 946419-58-5 (-)-D-1,5-bis-O-allyl-4-O-[2-(allyloxy)ethyl]-2,3,6-tris-O-benzyl-myo-inositol 
• 115102-31-3 2-(2-allyloxy-ethoxymethyl)-2-methyl-propane-1,3-diol 
• 2117-37-5 tri-n-butylgermanium bromide 
• 1180493-50-8 (C₅H₃NC₆H₄OCH₂CH₂OCH₂CHCH₂)2 
• 343945-22-2 C₁₃H₁₈O 

Relevant articles and documents

COMPOUNDS THAT INHIBIT MCL-1 PROTEIN

Provided herein are myeloid cell leukemia 1 protein (Mcl-1) inhibitors, methods of their preparation, related pharmaceutical compositions, and methods of using the same. For example, provided herein are compounds of Formula I, and pharmaceutically acceptable salts thereof and pharmaceutical compositions containing the compounds. The compounds and compositions provided herein may be used, for example, in the treatment of diseases or conditions, such as cancer.

The Reaction of Bis(dimethylglyoximato)(pyridine)cobalt(I), Cobaloxime(I), with 2-(Allyloxy)ethyl Halides and the Photolysis of the Resulting Organo-cobaloximes

The reactions of 2-(allyloxy)ethyl halides with cobaloxime(I) gave (tetrahydro-3-furanyl)methylcobaloximes via an electron transfer from cobaloxime(I) to the halides to give radical anions.The rupture of a halide ion to give an organic radical and the ring closure to give a (tetrahydro-3-furanyl)methyl radical are followed by the radical coupling between the organic radical and the cobaloxime(II).The structures of the organocobaloximes were determined by the analyses of the photolysis products under aerobic or anaerobic conditions.