116569-00-7

Basic information

• Product Name: 3-(Methoxycarbonyl)cyclobutanecarboxylicacid
• Synonyms: 3-(methoxycarbonyl)cyclobutane-1-carboxylic acid;1,3-Cyclobutanedicarboxylic acid monomethyl ester
• CAS NO: 116569-00-7
• Molecular Formula: C₇H₁₀O₄
• Molecular Weight: 158.1519
• Mol File: 116569-00-7.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 269.9±33.0 °C(Predicted)
• Appearance: /
• Density: 1.308±0.06 g/cm3(Predicted)
• PKA: 4.45±0.40(Predicted)
• CAS DataBase Reference: 3-(Methoxycarbonyl)cyclobutanecarboxylicacid(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(Methoxycarbonyl)cyclobutanecarboxylicacid(116569-00-7)
• EPA Substance Registry System: 3-(Methoxycarbonyl)cyclobutanecarboxylicacid(116569-00-7)

Safety Data

• Hazardous Substances Data: 116569-00-7(Hazardous Substances Data)

Usage

General Description

3-(Methoxycarbonyl)cyclobutanecarboxylic acid is a chemical compound with the molecular formula C8H12O4. It is a derivative of cyclobutanecarboxylic acid with a methoxycarbonyl functional group attached to the third carbon atom. 3-(Methoxycarbonyl)cyclobutanecarboxylicacid is commonly used as a building block in organic synthesis and pharmaceutical research. It has potential applications in the development of new drugs and other bioactive compounds due to its unique structure and reactivity. Additionally, it may be utilized in the production of specialty chemicals and materials for various industrial purposes.

Upstream product

• 67-56-1 methanol 
• 4462-97-9 cis-cyclobutane-1,3-dicarboxylic acid anhydride 
• 61752-11-2 methyl 3-oxo-2-oxabicyclo<2.2.0>hept-5-ene-6-carboxylate 
• 6018-41-3 methyl coumalate 
• 142733-60-6 2,2‐diethyl 7‐phenyl‐6,8‐dioxaspiro[3.5]nonane‐2,2‐dicarboxylate 
• 7371-69-9 1,1,3,3-cyclobutanetetracarboxylic acid 
• 77614-64-3 7‐phenyl‐6,8‐dioxaspiro[3.5]nonane‐2,2‐dicarboxylic acid 
• 4462-97-9 cis-1,3-Cyclobutandicarbonsaeureanhydrid 

Downstream Products

• 1349709-10-9 C₂₃H₂₆O₉ 
• 1363332-44-8 C₃₃H₃₆N₂O₉ 
• 1346648-43-8 C₁₄H₁₇NO₃S 
• 142733-63-9 cis-methyl 3-<(t-butoxycarbonyl)amino>cyclobutanecarboxylate 
• 142733-62-8 cis-methyl 3-carboxamidocyclobutanecarboxylate 
• 2398-17-6 cis-Methyl-3-hydroxymethyl-cyclobutan-carboxylat 

Relevant articles and documents

Scale-up synthesis of a deuterium-labeled cis-cyclobutane-1,3-Dicarboxylic acid derivative using continuous photo flow chemistry

Continuous photo flow synthesis of tert-butyl 3-oxo-2-oxabicyclo[2.2.0]hex-5-ene-6-carboxylate (2b) from tert-butyl 2-oxo-2H-pyran-5-carboxylate (1b) has been investigated for scale-up synthesis of cis-3-(tert-butoxycarbonyl)-2,3,4-d3-cyclobuta

Total synthesis and structural revision of the piperarborenines: When photochemistry meets C-H activation

Activate and reiterate: The activation of C(sp3)-H bonds is a highly desirable transformation because molecular complexity can be increased at the expense of the most simple and readily available organic linkage. In recent contributions this ap

SYNTHESIS OF NEW CARBOCYCLIC ANALOGUES OF OXETANOCIN A AND OXETANOCIN G

The synthesis of cis-3-amino-1-cyclobutanemethanol has been performed in six steps (59.6percent yield) from cis-1,3-cyclobutanedicarboxylic anhydride.This allowed us to obtain two new carbocyclic analogues of oxetanocin A and oxetanocin G related to 7-deazaadenosine and 7-deazaguanosine.