1262034-09-2

Basic information

• Product Name: C₁₆H₂₁NO₃
• Synonyms: C₁₆H₂₁NO₃
• CAS NO: 1262034-09-2
• Molecular Weight: 275.348
• Mol File: 1262034-09-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: C₁₆H₂₁NO₃(CAS DataBase Reference)
• NIST Chemistry Reference: C₁₆H₂₁NO₃(1262034-09-2)
• EPA Substance Registry System: C₁₆H₂₁NO₃(1262034-09-2)

Safety Data

• Hazardous Substances Data: 1262034-09-2(Hazardous Substances Data)

Upstream product

• 24424-99-5 di-tert-butyl dicarbonate 
• 615-43-0 2-iodophenylamine 
• 161117-84-6 tert-butyl 2-iodophenylcarbamate 
• 18857-02-8 3-methoxybut-1-yne 

Relevant articles and documents

PHOTOPROTECTIVE COMPOSITIONS CONTAINING MALASSEZIA-DERIVED COMPOUNDS AND/OR CHEMICAL ANALOGS THEREOF

The present invention relates to compounds, compositions, and methods for modulating skin pigmentation and treating or preventing UV-induced skin damage, erythema, aging of the skin, sunburn, and hyperpigmentation in a subject. The compounds, compositions, and methods of the present invention generally involve Malassezia-derived compounds, including malassezin and indirubin, and/or chemical analogs thereof. Other applications of the compounds and compositions disclosed herein include, but are not limited to, improving hyperpigmentation caused by a hyperpigmentation disorder, inducing melanocyte apoptosis, and modulating arylhydrocarbon receptor (AhR) activity, melanogenesis, melanin production, melanosome biogenesis, melanosome transfer, melanocyte activity, and melanin concentration.

Platinum(II)-catalyzed generation and [3+2] cycloaddition reaction of α,β-unsaturated carbene complex intermediates for the preparation of polycyclic compounds

Pt(II)-catalyzed generation of unsaturated carbene complex intermediates from various propargyl ether derivatives based on electrophilic activation of alkynes was realized. These in situ generated unsaturated carbene complexes undergo [3+2] cycloaddition reaction with various vinyl ethers, leading to efficient formation of indoles, naphthols, and benzofuran fused with a five-membered ring in high yields.