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Structure

Ethyl 2-oxocyclohexanecarboxylate

CAS
1655-07-8
Catalog Number
ACM1655078
Category
Other Products
Molecular Weight
170.21
Molecular Formula
C9H14O3

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Specification

Synonyms
2-oxo-cyclohexanecarboxylicaciethylester;Ethyl 1-oxo-2-cyclohexanecarboxylate;Ethyl 2-cyclohexanone-1-carboxylate;Ethyl 2-oxo-1-cyclohexanecarboxylate;Ethyl 2-oxocylohexanecarboxylate;Ethyl 2-oxylcyclohexanecarboxylic;AKOS 91391;AKOS MSC-0386
Boiling Point
106°C11mm Hg(lit.)
Flash Point
185°F
Density
1.064g/mL at 25°C(lit.)
Hazard Statements
Xi
Safety Description
23-24/25-37/39-26-36
Supplemental Hazard Statements
H227

Downstream Synthesis Route 1

  • 124-42-5
  • 1655-07-8
  • 19178-21-3

Reference: [1] Patent: US5234936, 1993, A,

Downstream Synthesis Route 2

  • 143-37-3
  • 1655-07-8
  • 19178-21-3

Reference: [1] Journal of the American Chemical Society, 1952, vol. 74, p. 842
[2] Journal of the American Chemical Society, 1958, vol. 80, p. 6609,6611

Downstream Synthesis Route 3

  • 1655-07-8
  • 858279-01-3

Reference: [1] Helvetica Chimica Acta, 1945, vol. 28, p. 1684,1690

Downstream Synthesis Route 4

  • 143-37-3
  • 1655-07-8
  • 19178-21-3

Reference: [1]Journal of the American Chemical Society,1952,vol. 74,p. 842
[2]Journal of the American Chemical Society,1958,vol. 80,p. 6609,6611

Downstream Synthesis Route 5

  • 515-46-8
  • 1655-07-8
  • 55443-01-1

Reference: [1]Blümel, Marcus; Crocker, Reece D.; Harper, Jason B.; Enders, Dieter; Nguyen, Thanh V.
[Chemical Communications, 2016, vol. 52, # 51, p. 7958 - 7961]

Downstream Synthesis Route 6

  • 2969-81-5
  • 1655-07-8
  • 4606-07-9
  • 124355-49-3

Reference: [1]Current Patent Assignee: MAX-PLANCK-GESELLSCHAFT ZUR FÖRDERUNG DER WISSENSCHAFT E.V. - WO2017/59191, 2017, A1
Location in patent: Paragraph 00174-00178
[2]Alford, Vincent M.; Kamath, Anushree; Ren, Xiaodong; Kumar, Kunal; Gan, Qianwen; Awwa, Monaf; Tong, Michael; Seeliger, Markus A.; Cao, Jian; Ojima, Iwao; Sampson, Nicole S.
[ACS Chemical Biology, 2017, vol. 12, # 11, p. 2788 - 2803]
[3]Curd; Rose
[Journal of the Chemical Society, 1946, p. 362,365]
[4]Baker et al.
[Journal of Organic Chemistry, 1953, vol. 18, p. 133,136]
[5]Polonovski; Libermann
[Bulletin de la Societe Chimique de France, 1947, p. 1073]

* For details of the synthesis route, please refer to the original source to ensure accuracy.

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