反応 #4108846
関連文献 (1)
openreactiondata ↗doi:10.1039/C8SC04228D
反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-a2a0c107ed774fdf877383272f921199表示可能な構造データがありません
CCCCCCCCCCCCC#CC#CCCCCCCCCC(=O)O製品情報
10,12-Pentacosadiynoic acid (CAS 66990-32-7) product identity, structure identifiers and related reaction data for chemical intermediate research and sourcing review.
想定用途
専門的研究・工業用途限定
データベース ID 538433
安全上の注意
For professional research and industrial use only. Review the supplier safety data sheet before handling.
合成データ
10 反応 · 10 文献
反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-a2a0c107ed774fdf877383272f921199反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 10,12-pentacosadiynoic acid (10 gm, GFS Chemicals) was dissolved in a solution containing 10 ml methanol (HPLC grade) and 10 ml chloroform (HPLC grade). The solution was stirred at room temperature and 10 drops of neat sulfuric acid was added drop wise. The solution was warmed to 100° F. for 2 hour. The reaction mixture was purified using column chromatography. The product (MePDA) was dried using a rotovap and the material stored in a chloroform solution. The solid form of MePDA was very unstable to polymerization and therefore kept dissolved in organic solutions. The solution was warmed to 100° F. for 2 hour The reaction mixture was purified The product (MePDA) was dried The solid form of MePDA was very unstable to polymerization kept dissolved in organic solutions
ソース ID: ord-b2453d96b47543b990fbad02313c1a9d反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: Alcoholic Monomer Solution of TDA/PDA: 10,12-Tricosadiynoic acid (TDA, 6 gm GFS Chemicals) and 10,12-pentacosadiynoic acid (PDA, 0.9 gm GFS Chemicals) were dissolved in 60 ml ethanol (Fisher). The solution was slightly warmed and stirred. The solution (TDA/PDA) was filtered (Whatman No. 1) to remove residual polymer. Dye colorant could be added to the alcoholic monomer solution as an indicator. Standard organic solvent based dyes were added at 2 drops per ml. The solution was slightly warmed The solution (TDA/PDA) was filtered (Whatman No. 1) to remove residual polymer Dye colorant could be added to the alcoholic monomer solution as an indicator were added at 2 drops per ml
ソース ID: ord-af5005e6f13c4f7bb696258067e46415反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: Alcoholic Monomer Solution of TDA/PDA: 10,12-Tricosadiynoic acid (TDA, 6 gm GFS Chemicals) and 10,12-pentacosadiynoic acid (PDA, 0.9 gm GFS Chemicals) were dissolved in 60 ml ethanol (Fisher). The solution was slightly warmed and stirred. The solution (TDA/PDA) was filtered (Whatman No. 1) to remove residual polymer. Dye colorant could be added to the alcoholic monomer solution as an indicator. Standard organic solvent based dyes were added at 2 drops per ml. The solution was slightly warmed The solution (TDA/PDA) was filtered (Whatman No. 1) to remove residual polymer Dye colorant could be added to the alcoholic monomer solution as an indicator were added at 2 drops per ml
ソース ID: ord-af5005e6f13c4f7bb696258067e46415反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 10,12-pentacosadiynoic acid (10 gm, GFS Chemicals) was dissolved in a solution containing 10 ml methanol (HPLC grade) and 10 ml chloroform (HPLC grade). The solution was stirred at room temperature and 10 drops of neat sulfuric acid was added drop wise. The solution was warmed to 100° F. for 2 hour. The reaction mixture was purified using column chromatography. The product (MePDA) was dried using a rotovap and the material stored in a chloroform solution. The solid form of MePDA was very unstable to polymerization and therefore kept dissolved in organic solutions. The solution was warmed to 100° F. for 2 hour The reaction mixture was purified The product (MePDA) was dried The solid form of MePDA was very unstable to polymerization kept dissolved in organic solutions
ソース ID: ord-11dba3e3e74c4629987aabe15daa030d反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 10,12-pentacosadiynoic acid (10 gm, GFS Chemicals) was dissolved in a solution containing 10 ml methanol (HPLC grade) and 10 ml chloroform (HPLC grade). The solution was stirred at room temperature and 10 drops of neat sulfuric acid was added drop wise. The solution was warmed to 100° F. for 2 hour. The reaction mixture was purified using column chromatography. The product (MePDA) was dried using a rotovap and the material stored in a chloroform solution. The solid form of MePDA was very unstable to polymerization and therefore kept dissolved in organic solutions. The solution was warmed to 100° F. for 2 hour The reaction mixture was purified The product (MePDA) was dried The solid form of MePDA was very unstable to polymerization kept dissolved in organic solutions
ソース ID: ord-b2453d96b47543b990fbad02313c1a9d反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-a2a0c107ed774fdf877383272f921199反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: Alcoholic Monomer Solution of TDA/PDA: 10,12-Tricosadiynoic acid (TDA, 6 gm GFS Chemicals) and 10,12-pentacosadiynoic acid (PDA, 0.9 gm GFS Chemicals) were dissolved in 60 ml ethanol (Fisher). The solution was slightly warmed and stirred. The solution (TDA/PDA) was filtered (Whatman No. 1) to remove residual polymer. Dye colorant could be added to the alcoholic monomer solution as an indicator. Standard organic solvent based dyes were added at 2 drops per ml. The solution was slightly warmed The solution (TDA/PDA) was filtered (Whatman No. 1) to remove residual polymer Dye colorant could be added to the alcoholic monomer solution as an indicator were added at 2 drops per ml
ソース ID: ord-af5005e6f13c4f7bb696258067e46415反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 10,12-pentacosadiynoic acid (10 gm, GFS Chemicals) was dissolved in a solution containing 10 ml methanol (HPLC grade) and 10 ml chloroform (HPLC grade). The solution was stirred at room temperature and 10 drops of neat sulfuric acid was added drop wise. The solution was warmed to 100° F. for 2 hour. The reaction mixture was purified using column chromatography. The product (MePDA) was dried using a rotovap and the material stored in a chloroform solution. The solid form of MePDA was very unstable to polymerization and therefore kept dissolved in organic solutions. The solution was warmed to 100° F. for 2 hour The reaction mixture was purified The product (MePDA) was dried The solid form of MePDA was very unstable to polymerization kept dissolved in organic solutions
ソース ID: ord-11dba3e3e74c4629987aabe15daa030d反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 10,12-pentacosadiynoic acid (10 gm, GFS Chemicals) was dissolved in a solution containing 10 ml methanol (HPLC grade) and 10 ml chloroform (HPLC grade). The solution was stirred at room temperature and 10 drops of neat sulfuric acid was added drop wise. The solution was warmed to 100° F. for 2 hour. The reaction mixture was purified using column chromatography. The product (MePDA) was dried using a rotovap and the material stored in a chloroform solution. The solid form of MePDA was very unstable to polymerization and therefore kept dissolved in organic solutions. The solution was warmed to 100° F. for 2 hour The reaction mixture was purified The product (MePDA) was dried The solid form of MePDA was very unstable to polymerization kept dissolved in organic solutions
ソース ID: ord-b2453d96b47543b990fbad02313c1a9dPubChem References
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