93007-95-5

Basic information

• Product Name: 1H-Inden-2-ol, 2,3-dihydro-1-[(phenylmethyl)amino]-
• CAS NO: 93007-95-5
• Molecular Formula: C16H17NO
• Molecular Weight: 239.317
• Mol File: 93007-95-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1H-Inden-2-ol, 2,3-dihydro-1-[(phenylmethyl)amino]-(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Inden-2-ol, 2,3-dihydro-1-[(phenylmethyl)amino]-(93007-95-5)
• EPA Substance Registry System: 1H-Inden-2-ol, 2,3-dihydro-1-[(phenylmethyl)amino]-(93007-95-5)

Safety Data

• Hazardous Substances Data: 93007-95-5(Hazardous Substances Data)

Upstream product

• 136030-00-7 (1R,2S)-1-Amino-2-indanol 
• 100-39-0 benzyl bromide 
• 95-13-6 1-indene 
• 100-46-9 benzylamine 
• 768-22-9 2,3-epoxyindene 
• 7480-35-5 trans-1-aminoindan-2-ol 
• 100-52-7 benzaldehyde 
• 10368-44-2 trans-2-bromo-1-indanol 

Relevant articles and documents

Nickel-Catalyzed Regio- And Stereospecific C-H Coupling of Benzamides with Aziridines

A nickel-catalyzed C-H coupling of 8-aminoquinoline-derived benzamides with aryl- and alkyl-substituted aziridines has been disclosed. The current strategy provides direct access to benzolactams by the C-H alkylation-intramolecular amidation cascade event with the concomitant removal of the aminoquinoline auxiliary. The regioselectivity of ring opening of aziridines can be controlled by the substituents. The reaction with chiral aziridines proceeds with inversion of configuration, thus suggesting an SN2-type nucleophilic ring-opening pathway.

Targeting multimeric imaging agents through multilocus binding

The present invention relates to contrast agents for diagnostic imaging. In particular, this invention relates to novel multimeric compounds which exhibit improved relaxivity properties upon binding to endogenous proteins or other physiologically relevant