4100-80-5

  • Product Name:Methylsuccinic Anhydride
  • Molecular Formula:C5H6O3
  • Purity:99%
  • Molecular Weight:114.101
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Product Details;

CasNo: 4100-80-5

Molecular Formula: C5H6O3

factory and supplier 4100-80-5 Methylsuccinic Anhydride in stock

  • Molecular Formula:C5H6O3
  • Molecular Weight:114.101
  • Vapor Pressure:0.0411mmHg at 25°C 
  • Melting Point:33-35 °C(lit.) 
  • Refractive Index:1.452 
  • Boiling Point:239 °C at 760 mmHg 
  • Flash Point:108.2 °C 
  • PSA:43.37000 
  • Density:1.23 g/cm3 
  • LogP:0.09600 

METHYLSUCCINIC ANHYDRIDE(Cas 4100-80-5) Usage

Definition

ChEBI: A tetrahydrofurandione that is succinic anhydride substituted by a methyl group at position 3.

InChI:InChI=1/C5H6O3/c1-3-2-4(6)8-5(3)7/h3H,2H2,1H3/t3-/m0/s1

4100-80-5 Relevant articles

-

Bergmann,Blum-Bergmann

, p. 1573 (1937)

-

Carbonylative Polymerization of Epoxides Mediated by Tri-metallic Complexes: A Dual Catalysis Strategy for Synthesis of Biodegradable Polyhydroxyalkanoates

Li, Wen-Bing,Liu, Ye,Lu, Xiao-Bing,Yang, Jin-Chuang,Yang, Jun

supporting information, (2022/01/20)

Polyhydroxyalkanoates (PHAs) are a uniqu...

Synthesis of Cyclic Anhydrides via Ligand-Enabled C–H Carbonylation of Simple Aliphatic Acids

Herron, Alastair N.,Yu, Jin-Quan,Zhuang, Zhe

supporting information, p. 16382 - 16387 (2021/06/23)

The development of C(sp3)–H functionaliz...

Thiol–Anhydride Dynamic Reversible Networks

Podgórski, Maciej,Mavila, Sudheendran,Huang, Sijia,Spurgin, Nathan,Sinha, Jasmine,Bowman, Christopher N.

supporting information, p. 9345 - 9349 (2020/04/07)

The reaction of thiols and anhydrides to...

(Meth) acrylic ester and manufacturing method thereof (by machine translation)

-

Paragraph 0058, (2019/12/04)

(Meth) acrylic acid ester of [be] hydrop...

4100-80-5 Process route

2-methylbutanedioic acid
498-21-5,636-60-2

2-methylbutanedioic acid

2-methylsuccinic anhydride
4100-80-5

2-methylsuccinic anhydride

Conditions
Conditions Yield
With oxalyl dichloride; N,N-dimethyl-formamide; In toluene; for 3h; Inert atmosphere; Reflux;
96%
With acetic anhydride; for 4h; Reflux;
88.2%
With acetyl chloride;
at 200 ℃; inactive form;
With diphosphorus pentasulfide; inactive form;
With acetyl chloride; inactive form;
With acetic anhydride;
With oxalyl dichloride; for 0.333333h; Heating;
With 4-methyl-morpholine; methyl chloroformate; In tetrahydrofuran; at 20 ℃; for 0.25h;
at 66.9 ℃; Equilibrium constant; Thermodynamic data; -ΔΔH;
With acetyl chloride;
4-methyloxetan-2-one
3068-88-0,32082-74-9,36536-46-6,65058-82-4

4-methyloxetan-2-one

carbon monoxide
201230-82-2

carbon monoxide

2-methylsuccinic anhydride
4100-80-5

2-methylsuccinic anhydride

Conditions
Conditions Yield
With ({1,2-di[(2-OH-3,5-di-tBu)PhCH=N]Ph}Al[THF]2)+[Co(CO)4]-; In toluene; at 55 ℃; for 24h; under 10343 Torr;
95%
[(meso-tetra(4-Cl-C6H4)porphyrinato)Al(THF)2]+[Co(CO)4]-; In 1,4-dioxane; at 40 ℃; under 43958.7 Torr; Further Variations:; Solvents; Pressures; Kinetics;
With Co(CO)4?Cr-MIL-101 MOF; silicon carbide powder; In toluene; at 40 ℃; for 60h; under 22502.3 Torr; Pressure; Temperature; chemoselective reaction; Catalytic behavior; Mechanism; Inert atmosphere; Glovebox; Flow reactor;

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