Butanedioic acid, trimethyl-

Base Information

• Chemical Name: Butanedioic acid, trimethyl-
• CAS No.: 2103-16-4
• Molecular Formula: C7H12O4
• Molecular Weight: 160.17
• European Community (EC) Number: 630-694-6
• NSC Number: 81626
• DSSTox Substance ID: DTXSID401030733
• Mol file: 2103-16-4.mol

Synonyms:Butanedioic acid, trimethyl-;2103-16-4;Trimethyl butanedioic acid;2,2,3-Trimethylsuccinic acid;NSC81626;2,2,3-trimethylbutanedioic acid;Trimethylbernsteinsaure;NCIOpen2_000794;SCHEMBL2784566;DTXSID401030733;NSC 81626;NSC-81626;Benzenepropanoic acid, .alpha., .beta.-dicyano-.beta.-phenyl-.alpha.-(phenylmethyl)-;2,3-Butanedicarboxylic acid, 2-methyl-;Benzenepropanoic acid,.beta.-dicyano-.beta.-phenyl-.alpha.-(phenylmethyl)-;Benzenepropanoic acid, .alpha.,.beta.-dicyano-.beta.-phenyl-.alpha.-(phenylmethyl)-

Chemical Property of Butanedioic acid, trimethyl-

Chemical Property:

• Vapor Pressure: 0.00705mmHg at 25°C
• Boiling Point: 250°Cat760mmHg
• Flash Point: 119.2°C
• Density: 1.197g/cm³
• XLogP3: 0.7
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 3
• Exact Mass: 160.07355886
• Heavy Atom Count: 11
• Complexity: 183

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC(C(=O)O)C(C)(C)C(=O)O

Technology Process of Butanedioic acid, trimethyl-

There total 6 articles about Butanedioic acid, trimethyl- which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

(-)-α-cedrene (469-61-4) + acetone (67-64-1) → 2,3,3-trimethylsuccinic acid (2103-16-4) + 3-methylbutane-1,2,3-tricarboxylic acid (77370-41-3) + succinic acid (110-15-6) + 2,2-dimethylmalonic acid (595-46-0)

Guidance literature:

anschliessend Behandeln mit wss. HNO₃ in Essigsaeure;

Reference yield:

ethyl 2-bromoisovalerate (609-12-1) → 2,3,3-trimethylsuccinic acid (2103-16-4) + 2,2-dimethylglutaric acid (681-57-2)

Guidance literature:

With xylene; man verseift das Reaktionsprodukt mit alkoholischer Kalilauge und die durch Salzsaeure in Freiheit gesetzten Saeuren auf 200grad bis zum Aufhoeren der Kohlensaeureentwicklung erhitzt;

Reference yield:

ethyl 2-bromoisovalerate (609-12-1) → 2,3,3-trimethylsuccinic acid (2103-16-4) + 2,2-dimethylglutaric acid (681-57-2)

Guidance literature:

With ethanol; sodium ethanolate; Kochen des Reaktionsprodukts mit Schwefelsaeure;

upstream raw materials:

ethyl 2-bromoisovalerate

D-(+)-camphoric acid

water

(-)-α-cedrene