91444-55-2

Basic information

• Product Name: 1H-Indol-5-ol, 2-[4-(acetyloxy)phenyl]-3-methyl-, acetate (ester)
• CAS NO: 91444-55-2
• Molecular Formula: C19H17NO4
• Molecular Weight: 323.348
• Mol File: 91444-55-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1H-Indol-5-ol, 2-[4-(acetyloxy)phenyl]-3-methyl-, acetate (ester)(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Indol-5-ol, 2-[4-(acetyloxy)phenyl]-3-methyl-, acetate (ester)(91444-55-2)
• EPA Substance Registry System: 1H-Indol-5-ol, 2-[4-(acetyloxy)phenyl]-3-methyl-, acetate (ester)(91444-55-2)

Safety Data

• Hazardous Substances Data: 91444-55-2(Hazardous Substances Data)

Upstream product

• 64-19-7 acetic acid 
• 91444-54-1 2-(4-hydroxyphenyl)-3-methyl-1H-indol-5-ol 
• 75-36-5 acetyl chloride 
• 104-94-9 4-methoxy-aniline 
• 25743-57-1 1-(4-acetoxy-phenyl)-2-bromo-propan-1-one 
• 2623-33-8 4-acetoxyacetanilide 
• 91444-18-7 5-methoxy-2-(4-methoxyphenyl)-3-methyl-1H-indole 
• 21086-33-9 2-bromo-1-(4-methoxyphenyl)-1-propanone 
• 108-24-7 acetic anhydride 

Downstream Products

• 198481-32-2 bazedoxifene 

Relevant articles and documents

METHODS OF PREPARING　BAZOEDOXIFENE

The present invention relates to novel bazedoxifene or to a method for producing a pharmaceutically acceptable salt thereof. The production method according to the present invention can provide the bazedoxifene with high purity and high yield, and is economical and environmentally friendly in terms of time and cost due to a relatively simple manufacturing process to be usefully applied to mass production.COPYRIGHT KIPO 2018

2-Phenylindoles. Relationship between Structure, Estrogen Receptor Affinity, and Mammary Tumor Inhibiting Activity in the Rat

A number of 2-phenylindole derivatives with one hydroxy group in the meta or para position of the phenyl ring and a second one in position 5, 6, or 7 of the indole nucleus were synthesized.In addition, different alkyl groups were introduced into positions