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| cis-4-シクロヘキセン-1,2-ジカルボン酸無水物 製品概要 |
化学名: | cis-4-シクロヘキセン-1,2-ジカルボン酸無水物 | 英語化学名: | cis-1,2,3,6-Tetrahydrophthalic anhydride | 别名: | 1,3-isobenzofurandion,3a,4,7,7a-tetrahydro-,cis-;3-Isobenzofurandione,3a,4,7,7a-tetrahydro-,cis-1;4,7,7a-tetrahydro-3-isobenzofurandioncis-3a;cis-3a,4,7,7a-Tetrahydro-1,3-isobenzofurandione;CIS-THPA;CIS-DELTA4-TETRAHYDROPHTHALIC ANHYDRIDE;CIS-4-TETRAHYDROPHTHALIC ANHYDRIDE;CIS-1,2,3,6-TETRAHYDROPHTHALIC ANHYDRIDE | CAS番号: | 935-79-5 | 分子式: | C8H8O3 | 分子量: | 152.15 | EINECS: | 213-308-7 | カテゴリ情報: | Diels-Alder Adducts | Mol File: | 935-79-5.mol | |
| cis-4-シクロヘキセン-1,2-ジカルボン酸無水物 物理性質 |
融点 | 98 °C | 沸点 | 234.6°C (rough estimate) | 比重(密度) | 1.2143 (rough estimate) | 蒸気密度 | 5.2 (vs air) | 蒸気圧 | <0.01 mm Hg ( 20 °C) | 屈折率 | 1.4447 (estimate) | 闪点 | 156 °C | 貯蔵温度 | under inert gas (nitrogen or Argon) at 2-8°C | 溶解性 | soluble in Toluene,Benzene | 外見 | powder to crystal | 色 | White to Almost white | 水溶解度 | REACTS | Sensitive | Moisture Sensitive | BRN | 82341 | 暴露限界値 | ACGIH: TWA 0.01 mg/m3 OSHA: TWA 0.25 ppm(1 mg/m3) NIOSH: IDLH 10 mg/m3; TWA 0.25 ppm(1 mg/m3) | CAS データベース | 935-79-5(CAS DataBase Reference) | NISTの化学物質情報 | cis-1,2,3,6-Tetrahydrophthalic anhydride(935-79-5) | EPAの化学物質情報 | 1,3-Isobenzofurandione, 3a,4,7,7a-tetrahydro-, (3aR,7aS)-rel- (935-79-5) |
| cis-4-シクロヘキセン-1,2-ジカルボン酸無水物 Usage And Synthesis |
外観 | 白色~わずかにうすい黄色, フレーク | 溶解性 | 水に難溶, エタノールに可溶。熱エタノール(99.5)に溶ける。ベンゼンに可溶。エーテル、石油エーテルに微溶。 | 説明 | Tetrahydrophthalic anhydride is an organic compound with the formula C6H8C2O3. The compound exists as two isomers, this article being focused on the more common cis isomer. It is a precursor to other compounds including the dicarboxylic acid tetrahydrophthalic acid as well the tetrahydrophthalimide, which is a precursor to the fungicide Captan. It is a white solid that is soluble in organic solvents. Tetrahydrophthalic anhydride, the cis isomer, is prepared by the Diels-Alder reaction of butadiene and maleic anhydride. | 化学的特性 | Tetrahydrophthalic Anhydride (THPA) is a white crystalline powder or FLAKES. It is slightly soluble in benzene and acetone and it is also sensitive to moisture. | 使用 | cis-1,2,3,6-Tetrahydrophthalic anhydride (THPA) can be used as:
- A curing agent for epoxides.
- A chemical modifier in the modification of polystyrene via Friedel-Crafts acylation for enhancing the thermal stability of the polymer.
- A reactant for the synthesis of cis-tetrahydroisoindole-1,3-dione derivatives and cyclic diimides.
| 使用 | Tetrahydrophthalic Anhydride is an anhydride hardener mainly used in the fields of coatings, epoxy resin curing agents, polyester resins, adhesives, plasticizers, pesticides, etc. It is also used as a chemical intermediate for light colored alkyds. Tetrahydrophthalic Anhydride is an organic compound obtained from the reaction of Maleic Anhydride and Butadiene. | 製造方法 | A flask containing 500 ml of dry benzene and 196 gm (2 moles) of maleic anhydride is heated with a pan of hot water while butadiene is introduced rapidly (0.6-0.8 liter/min) from a commercial cylinder. The solution is stirred rapidly and the heating is stopped after 3-5 min when the temperature reaches 50°C. In 15-25 min the reaction causes the temperature of the solution to reach 70-75°C. The absorption of the rapid stream of butadiene is nearly complete in 30-40 min. The addition of butadiene is continued at a slower rate for a total of 2\ hr. The solution is poured into a 1-liter beaker which is covered and kept at 0-5°C overnight. The product is collected on a large Buchner funnel and washed with 250 ml of b.p. 35-60°C petroleum ether. A second crop is obtained by diluting the filtrate with an additional 250 ml of petroleum ether. Both crops are dried to constant weight in an oven at 70-80°C to yield 281.5-294.5 gm (96- 97%, m.p. 99-102°C). Recrystallization from ligroin or ether raises the melting point to 103-104°C.
| Synthesis Reference(s) | Journal of the American Chemical Society, 64, p. 802, 1942 DOI: 10.1021/ja01256a018 |
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