40614-27-5

Basic information

• Product Name: 4,4-dimethyl-3,4-dihydro-2H-chromene
• CAS NO: 40614-27-5
• Molecular Formula: C₁₁H₁₄O
• Molecular Weight: 162.2283
• Mol File: 40614-27-5.mol
• Article Data: 23

Chemical Properties

• Boiling Point: 231.9°C at 760 mmHg
• Flash Point: 87.1°C
• Density: 0.978g/cm³
• Vapor Pressure: 0.0924mmHg at 25°C
• Refractive Index: 1.507
• CAS DataBase Reference: 4,4-dimethyl-3,4-dihydro-2H-chromene(CAS DataBase Reference)
• NIST Chemistry Reference: 4,4-dimethyl-3,4-dihydro-2H-chromene(40614-27-5)
• EPA Substance Registry System: 4,4-dimethyl-3,4-dihydro-2H-chromene(40614-27-5)

Safety Data

• Hazardous Substances Data: 40614-27-5(Hazardous Substances Data)

Upstream product

• 58584-26-2 ((3-methylbut-3-en-1-yl)oxy)benzene 
• 40614-15-1 Methanesulfonic acid 3-(2-hydroxy-phenyl)-3-methyl-butyl ester 
• 87077-92-7 2-methyl-4-phenoxy-2-butanol 
• 42007-25-0 diphenyl 3-methyl-3-buten-1-yl phosphate 
• 108-95-2 phenol 
• 3350-78-5 3,3-Dimethylacryloyl chloride 
• 924-50-5 Methyl 3,3-dimethylacrylate 
• 763-32-6 2-methyl-1-buten-4-ol 
• 40614-20-8 3-(2'-Hydroxyphenyl)-3,3-dimethylpropanol 
• 54897-52-8 phenyl 3,3-dimethylacrylate 
• 29598-22-9 4,4-dimethyl-2-oxo-chroman 
• 7497-89-4 methyl 3-phenoxypropanoate 
• 7170-38-9 3-phenoxypropanoic acid 
• 81246-49-3 3-<2-((methylthio)methoxy)phenyl>-3,3-dimethyl-1-propanol 

Downstream Products

• 1027385-16-5 4-[(4,4-Dimethyl-9-oxo-3,4,6,7,8,9-hexahydro-2H-benzo[g]chromen-8-yl)-hydroxy-methyl]-benzoic acid methyl ester 
• 88579-23-1 3,4-dihydro-4,4-dimethyl-2H-1-benzothiopyran-6-yl methyl ketone 
• 127255-57-6 4-[(Z)-2-(4,4-Dimethyl-chroman-6-yl)-propenyl]-benzoic acid ethyl ester 
• 88579-22-0 [1-(4,4-dimethyl-6-chromanyl)ethyl]triphenylphosphonium bromide 
• 109140-01-4 methyl 4-<(4,4-dimethyl-6-chromanyl)carbamoyl>benzoate 
• 109140-02-5 4-<(4,4-dimethyl-6-chromanyl)carbamoyl>benzoic acid 
• 87077-92-7 2-methyl-4-phenoxy-2-butanol 

Relevant articles and documents

CHROMAN-SUBSTITUTED, TETRAHYDROQUINOLINE-SUBSTITUTED AND THIOCHROMAN-SUBSTITUTED HETEROAROTINOIDS AS ANTI-CANCER AGENTS

Chemical compounds that inhibit cancer cell growth are provided. The compounds are heteroarotinoids and derivatives thereof with oxygen, nitrogen or sulfur in chroman systems, tetrahydroquinoline systems, and tetrahydrothiochroman systems.

Co-Catalyzed Hydroarylation of Unactivated Olefins

A mild, general, scalable, and functional group tolerant intramolecular hydroarylation of unactivated olefins using a Co(salen) complex, a N-fluoropyridinium salt, and a disiloxane reagent was reported. This method, which was carried out at room temperature, afforded six-membered benzocyclic compounds from mono-, 1,1- or trans-1,2-di, and trisubstituted olefins.

HETEROCYCLIC GPR40 MODULATORS

The present invention provides compounds useful, for example, for treating metabolic disorders in a subject. Such compounds have the general formula I: where the definitions of the variables are provided herein. The present invention also provides compositions that include, and methods for using, the compounds in preparing medicaments and for treating metabolic disorders such as, for example, type II diabetes.