115609-04-6

Basic information

• Product Name: 1-(4-bromophenyl)-1-phenylpropargyl alcohol
• CAS NO: 115609-04-6
• Molecular Weight: 287.156
• Mol File: 115609-04-6.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 1-(4-bromophenyl)-1-phenylpropargyl alcohol(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(4-bromophenyl)-1-phenylpropargyl alcohol(115609-04-6)
• EPA Substance Registry System: 1-(4-bromophenyl)-1-phenylpropargyl alcohol(115609-04-6)

Safety Data

• Hazardous Substances Data: 115609-04-6(Hazardous Substances Data)

Upstream product

• 90-90-4 (4-bromophenyl)(phenyl)methanone 
• 70277-75-7 lithium acetylide 
• 1066-26-8 sodium acetylide 
• 1066-54-2 trimethylsilylacetylene 
• 4301-14-8 acetylenemagnesium bromide 

Downstream Products

• 1187363-44-5 3-(4-bromophenyl)-3-phenyl-3H-naphtho[2,1-b]pyran 
• 1292816-18-2 3-(4-bromophenyl)-2,5-diphenylfuran 
• 1393371-28-2 2-(4-bromophenyl)-3,5-diphenylfuran 
• 1393371-21-5 (4-(2-(4-bromophenyl)-2-phenylvinyl)-2,5-diphenylfuran-3-yl)(phenyl)methanone 
• 1393370-81-4 (4-(2-(4-bromophenyl)-2-phenylvinyl)-2,5-diphenylfuran-3-yl)(phenyl)methanone 
• 13632-24-1 1,6-di(p-bromophenyl)-1,6-diphenylhexa-2,4-diyne-1,6-diol 
• 10473-74-2 Carbamidsaeure-<1-(4-brom-phenyl)-1-phenyl-propin-(2)-ylester> 
• 10473-65-1 N-Methyl-carbamidsaeure-<1-(4-brom-phenyl)-1-phenyl-propin-(2)-ylester> 
• 10473-92-4 N,N-Dimethyl-carbamidsaeure-<1-(4-brom-phenyl)-1-phenyl-propin-(2)-ylester> 

Relevant articles and documents

Organic photochromic dyes and their use for dye-sensitized solar cells

The present invention concerns an organic dye comprising a photochromic entity, a segment -eD representing an electron donor segment and a segment -L-A with -L- representing a covalent bond or a spacer segment and particularly a pi-conjugated spacer segme

Bronsted acid-catalyzed cycloisomerization of but-2-yne-1,4-diols with or without 1,3-dicarbonyl compounds to tri- and tetrasubstituted furans

A Bronsted acid-catalyzed method to prepare tri- and tetrasubstituted furans efficiently from cycloisomerization of but-2-yne-1,4-diols with or without 1,3-dicarbonyl compounds is described. By taking advantage of the orthogonal modes of reactivity of the alcoholic substrate through slight modification of the reaction conditions, a divergence in product selectivity was observed. At room temperature, p-TsOH?H 2O-mediated tandem alkylation/cycloisomerization of the propargylic 1,4-diol with the β-dicarbonyl compound was found to selectively occur to provide the tetrasubstituted furan product. On the other hand, increasing the reaction temperature to 80 °C was discovered to result in preferential p-TsOH?H2O-catalyzed dehydrative rearrangement of the unsaturated alcohol and formation of the 2,3,5-trisubstituted furan adduct.

AMINO ALCOHOLS OF THE ACETYLENE SERIES. X. 1-PHENYL-1-SUBSTITUTED ARYL(HETARYL)-4-DIALKYLAMINO-2-BUTYN-1-OLS

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