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Cyclobutaneacetaldehyde, 3-formyl-2,2-dimethyl-, (1R,3R)- (9CI)

Base Information Edit
  • Chemical Name:Cyclobutaneacetaldehyde, 3-formyl-2,2-dimethyl-, (1R,3R)- (9CI)
  • CAS No.:288848-36-2
  • Molecular Formula:C9H14 O2
  • Molecular Weight:154.20626
  • Hs Code.:
  • Mol file:288848-36-2.mol
Cyclobutaneacetaldehyde, 3-formyl-2,2-dimethyl-, (1R,3R)- (9CI)

Synonyms:Cyclobutaneacetaldehyde, 3-formyl-2,2-dimethyl-, (1R,3R)- (9CI)

Suppliers and Price of Cyclobutaneacetaldehyde, 3-formyl-2,2-dimethyl-, (1R,3R)- (9CI)
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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of Cyclobutaneacetaldehyde, 3-formyl-2,2-dimethyl-, (1R,3R)- (9CI) Edit
Chemical Property:
  • PSA:34.14000 
  • LogP:1.43660 
Purity/Quality:
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  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

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Technology Process of Cyclobutaneacetaldehyde, 3-formyl-2,2-dimethyl-, (1R,3R)- (9CI)

There total 5 articles about Cyclobutaneacetaldehyde, 3-formyl-2,2-dimethyl-, (1R,3R)- (9CI) 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:
Guidance literature:
With oxalyl dichloride; dimethyl sulfoxide; triethylamine; In dichloromethane; at -50 - 20 ℃;
DOI:10.1021/jo991773c
Guidance literature:
Multi-step reaction with 4 steps
1: 70 percent / aq. NaOBr / dioxane / 0 - 20 °C
2: 96 percent / KOH / diethyl ether; ethanol / 1 h / 20 °C
3: 85 percent / LiBH4 / tetrahydrofuran / Heating
4: 70 percent / (COCl)2; DMSO; Et3N / CH2Cl2 / -50 - 20 °C
With potassium hydroxide; lithium borohydride; sodium hypobromide; oxalyl dichloride; dimethyl sulfoxide; triethylamine; In tetrahydrofuran; 1,4-dioxane; diethyl ether; ethanol; dichloromethane; 1: Oxidation / 2: Methylation / 3: Reduction / 4: Oxidation;
DOI:10.1021/jo991773c
Guidance literature:
Multi-step reaction with 3 steps
1: 96 percent / KOH / diethyl ether; ethanol / 1 h / 20 °C
2: 85 percent / LiBH4 / tetrahydrofuran / Heating
3: 70 percent / (COCl)2; DMSO; Et3N / CH2Cl2 / -50 - 20 °C
With potassium hydroxide; lithium borohydride; oxalyl dichloride; dimethyl sulfoxide; triethylamine; In tetrahydrofuran; diethyl ether; ethanol; dichloromethane; 1: Methylation / 2: Reduction / 3: Oxidation;
DOI:10.1021/jo991773c
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