38841-00-8

Basic information

• Product Name: 1α,2α,3β,4β-Cyclobutanetetracarboxylic acid
• Synonyms: 1,2,3,4-Cyclobutanetetracarboxylic acid, (1α,2α,3β,4β)-;1,2-cis-2,3-trans-3,4-cis-cyclobutane-1,2,3,4-tetracarboxylic acid
• CAS NO: 38841-00-8
• Molecular Formula: C₈H₈O₈
• Molecular Weight: 232.14
• Mol File: 38841-00-8.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1α,2α,3β,4β-Cyclobutanetetracarboxylic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 1α,2α,3β,4β-Cyclobutanetetracarboxylic acid(38841-00-8)
• EPA Substance Registry System: 1α,2α,3β,4β-Cyclobutanetetracarboxylic acid(38841-00-8)

Safety Data

• Hazardous Substances Data: 38841-00-8(Hazardous Substances Data)

Downstream Products

• 54120-37-5 cis,trans,cis-1,2,3,4-Tetrabenzoyl-cyclobutan 
• 98879-38-0 trans,trans,trans-1,2,3,4-Tetrakis-(hydroxy-phenyl-methyl)-cyclobutan 
• 54120-37-5 trans,trans,trans-1,2,3,4-Tetrabenzoyl-cyclobutan 
• 99174-47-7 trans,trans,trans-1.2.3.4-tetra-(α-Hydroxy-benzhydryl)-cyclobutan 
• 96507-49-2 trans,trans,trans-1,2,3,4-Tetrabenzyl-cyclobutan 

Relevant articles and documents

Coerced photodimerization reaction in the solid state through amine salt formation

Photodimerization of fumaric or several γ-form trans-cinnamic acids proceeded successfully in the solid state through amine salt formation with ammonia or some aromatic heterocyclic amines (especially, imidazole). It appears that this success is due to a small size or a planar structure of the amine. A layered or a channel-type clathrate crystal structure was revealed, respectively.