16657-10-6

Basic information

• Product Name: 4-BROMO-2,3-DIHYDRO-1H-INDEN-1-OL
• Synonyms: 4-BROMO-2,3-DIHYDRO-1H-INDEN-1-OL;4-Bromoindan-1-ol;4-Bromo-1-indanol;4-Bromo-1-indanol 97%;1H-Inden-1-ol, 4-bromo-2,3-dihydro-;1H-Inden-1-ol, 4-bromo-2,3-dihydro-
• CAS NO: 16657-10-6
• Molecular Formula: C₉H₉BrO
• Molecular Weight: 213.08
• Mol File: 16657-10-6.mol
• Article Data: 17

Chemical Properties

• Melting Point: 72℃
• Appearance: /
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: 4-BROMO-2,3-DIHYDRO-1H-INDEN-1-OL(CAS DataBase Reference)
• NIST Chemistry Reference: 4-BROMO-2,3-DIHYDRO-1H-INDEN-1-OL(16657-10-6)
• EPA Substance Registry System: 4-BROMO-2,3-DIHYDRO-1H-INDEN-1-OL(16657-10-6)

Safety Data

• Hazard Codes: Xn
• Statements: 22
• WGK Germany: 1
• Hazardous Substances Data: 16657-10-6(Hazardous Substances Data)

Usage

General Description

4-Bromo-2,3-dihydro-1H-inden-1-ol is a chemical compound that belongs to the family of organic compounds known as phenols. It is a colorless to light yellow liquid with a pungent odor. 4-BROMO-2,3-DIHYDRO-1H-INDEN-1-OL is primarily used as an intermediate in the synthesis of pharmaceuticals and other organic compounds. It is also used as a building block in the production of specialty chemicals and agrochemicals. 4-Bromo-2,3-dihydro-1H-inden-1-ol is also used in the manufacturing of fragrances and flavors due to its unique aromatic properties. It is important to handle this compound with care, as it is considered to be hazardous to human health and the environment.

Upstream product

• 335159-82-5 3-(m-bromophenyl)propionyl chloride 
• 42287-90-1 3-(3-bromophenyl)propanoic acid 
• 3433-80-5 1-Bromo-2-bromomethyl-benzene 
• 58380-12-4 <(2-bromophenyl)methyl>propanedicarboxylic acid 
• 15115-58-9 3-(2-bromophenyl)propionic acid 
• 66192-11-8 diethyl 2-(2-bromobenzyl)propan-1,3-dioate 
• 90725-40-9 3-(2-bromophenyl)propanoyl chloride 
• 15115-60-3 4-bromo-2,3-dihydroinden-1-one 

Downstream Products

• 78383-18-3 4-phenyl-2,3-dihydro-1H-inden-1-ol 
• 124067-30-7 4-Methoxy-indan-2-one 
• 125141-73-3 4-bromo-2,3-dihydro-1H-inden-2-ol 
• 846032-36-8 4-bromo-1,3-dihydro-2H-inden-2-one 
• 83808-19-9 (1S)-4-bromo-2,3-dihydro-1H-inden-1-ol 

Relevant articles and documents

Total Synthesis of Viridin and Viridiol

The asymmetric total synthesis of (-)-viridin and (-)-viridiol, antifungal metabolites, was achieved in 17 and 18 steps from a commercially available starting material. An intramolecular [3+2] cycloaddition was applied to an easily available l-ribose derivative in order to construct the highly substituted D ring containing the key chiral cis-triol fragment. Co-catalyzed metal-hydride H atom transfer (MHAT) radical cyclization was utilized to form the C-ring and the all-carbon quaternary center at C-10. This convergent strategy provides a scalable approach to prepare viridin and viridiol for biological studies.

S1P1 AGONIST AND APPLICATION THEREOF

The present invention relates to a class of tricyclic compounds and an application thereof as a sphingosine 1-phosphate type 1 (S1P1) receptor agonist. The invention specifically relates to a compound represented by formula (II), and a tautomer and pharmaceutically acceptable salt of same.

Aromatic ring-containing compound and application thereof

The present invention discloses an aromatic ring-containing compound and an application thereof, and provides an aromatic ring-containing compound represented by formula I, and a pharmaceutically acceptable salt, a hydrate, a solvate, a metabolite, a ster