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935-79-5

  • Product NameCis-1,2,3,6-tetrahydrophthalic anhydride
  • Molecular FormulaC8H8 O3
  • Molecular Weight152.15
  • Purity99%
  • Appearancewhite flakes
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Product Details

Quick Details

  • CasNo: 935-79-5
  • Molecular Formula: C8H8 O3
  • Appearance: white flakes
  • Purity: 99%

Hot Sale Best Quality Top Purity Industrial Grade 935-79-5 Specifications Powder with Cheap Price, In Bulk Supply, Fast Delivery

  • Molecular Formula:C8H8 O3
  • Molecular Weight:152.15
  • Appearance/Colour:white flakes 
  • Vapor Pressure:<0.01 mm Hg ( 20 °C) 
  • Melting Point:98 °C 
  • Refractive Index:1.529 
  • Boiling Point:305.6 °C at 760 mmHg 
  • Flash Point:148.2 °C 
  • PSA:43.37000 
  • Density:1.289 g/cm3 
  • LogP:0.65220 

cis-1,2,3,6-Tetrahydrophthalic anhydride(Cas 935-79-5) Usage

Preparation

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

InChI:InChI=1/C8H8O3/c9-7-5-3-1-2-4-6(5)8(10)11-7/h1,3,5-6H,2,4H2

935-79-5 Relevant articles

cis-1,2,3,6-Tetrahydrophthalic anhydride at 173 K

Bolte, Michael,Bauch, Christian

, p. 226 - 228 (1999)

The title compound, C8H8O1, (I), crystal...

-

Weininger et al.

, p. 3732 (1964)

-

Novel 1,2,3-triazole compounds: Synthesis, In vitro xanthine oxidase inhibitory activity, and molecular docking studies

Tan, Ayse

, (2020/03/25)

In this study, novel 1,2,3-triazole comp...

An anomalous addition of chlorosulfonyl isocyanate to a carbonyl group: The synthesis of ((3aS,7aR,E)-2-ethyl-3-oxo-2,3,3a,4,7,7a-hexahydro-1H-isoindol-1-ylidene)sulfamoyl chloride

K?se, Aytekin,ünal, Asli,?ahin, Ertan,Bozkaya, U?ur,Kara, Yunus

, p. 931 - 936 (2019/06/08)

In this study, we developed a new additi...

Access to amphiphilic cis-configurated polyamide-3 using alcohols as initiators

Maiatska, Olga,Belkin, Alexander,Ritter, Helmut

, p. 2367 - 2369 (2015/05/13)

The synthesis of polyamide-3 from 4a,5,8...

Tandem Diels-Alder/cross-coupling reactions of generated in situ organoindium reagents in a one-pot process

Mo, Juntae,Kim, Sung Hong,Lee, Phil Ho

supporting information; experimental part, p. 424 - 427 (2010/04/24)

[Chemical equation presented] Tandem Die...

935-79-5 Process route

maleic anhydride
108-31-6

maleic anhydride

4-bromo-buta-1,2-diene
18668-68-3

4-bromo-buta-1,2-diene

cis-1,2,3,6-tetrahydrophthalic anhydride
935-79-5

cis-1,2,3,6-tetrahydrophthalic anhydride

Conditions
Conditions Yield
4-bromo-buta-1,2-diene; With indium; In N,N-dimethyl-formamide; at 20 ℃; for 0.5h; Inert atmosphere;
maleic anhydride; In N,N-dimethyl-formamide; at 80 ℃; for 2h; Inert atmosphere;
With water; sodium hydrogencarbonate; In N,N-dimethyl-formamide; Inert atmosphere;
83%
maleic anhydride
108-31-6

maleic anhydride

3-Sulfolene
77-79-2

3-Sulfolene

cis-1,2,3,6-tetrahydrophthalic anhydride
935-79-5

cis-1,2,3,6-tetrahydrophthalic anhydride

Conditions
Conditions Yield
In benzene; at 100 ℃; for 5h;
86%
With hydroquinone; In toluene; at 120 ℃; in sealed bomb reactor;
 
In xylene; Heating;
 
In toluene; Reflux;
 
In 5,5-dimethyl-1,3-cyclohexadiene; Reflux;
 

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    3-Sulfolene

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    buta-1,3-diene

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