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[ CAS No. 29655-79-6 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
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Type HazMat fee for 500 gram (Estimated)
Excepted Quantity USD 0.00
Limited Quantity USD 15-60
Inaccessible (Haz class 6.1), Domestic USD 80+
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Chemical Structure| 29655-79-6
Chemical Structure| 29655-79-6
Structure of 29655-79-6 * Storage: {[proInfo.prStorage]}
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Product Details of [ 29655-79-6 ]

CAS No. :29655-79-6 MDL No. :MFCD00831071
Formula : C8H13NO5 Boiling Point : -
Linear Structure Formula :- InChI Key :WFXMDHFQXBWTSB-UHFFFAOYSA-N
M.W : 203.19 Pubchem ID :2779372
Synonyms :

Safety of [ 29655-79-6 ]

Signal Word:Danger Class:9
Precautionary Statements:P260-P264-P273-P301+P312-P305+P351+P338-P314 UN#:3082
Hazard Statements:H302-H319-H372-H410 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 29655-79-6 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Upstream synthesis route of [ 29655-79-6 ]
  • Downstream synthetic route of [ 29655-79-6 ]

[ 29655-79-6 ] Synthesis Path-Upstream   1~7

  • 1
  • [ 623-33-6 ]
  • [ 4755-77-5 ]
  • [ 29655-79-6 ]
YieldReaction ConditionsOperation in experiment
51% With triethylamine In dichloromethane Example 2 Ii; Compound 4 was prepared according to the Ref: J. Hetero. Chem. 1995, 32, 1693-1702. Then, it was reduced by NaBH4ZLiCl in ethanol solution. Further oxidation by Dess-Martin reagent gave the desired aldehyde 6 in 25 percent overall two-step yield.
Reference: [1] Synthetic Communications, 2000, vol. 30, # 17, p. 3171 - 3180
[2] Patent: WO2007/124546, 2007, A1, . Location in patent: Page/Page column 63
[3] Chemische Berichte, 1897, vol. 30, p. 590
[4] Journal of the American Chemical Society, 1997, vol. 119, # 1, p. 86 - 93
[5] Organic Process Research and Development, 2004, vol. 8, # 2, p. 192 - 200
  • 2
  • [ 95-92-1 ]
  • [ 459-73-4 ]
  • [ 29655-79-6 ]
Reference: [1] Bioorganic and Medicinal Chemistry Letters, 2002, vol. 12, # 8, p. 1203 - 1208
[2] Acta Chemica Scandinavica, 1999, vol. 53, # 7, p. 521 - 527
  • 3
  • [ 924-44-7 ]
  • [ 29655-79-6 ]
YieldReaction ConditionsOperation in experiment
60% With ammonium acetate In tetrahydrofuran at 66℃; for 8 h; General procedure: To the solution of isopropyl glyoxylate (1.28 g, 11 mmol) in THF (50 mL), ammonium acetate (3 equiv., 2.55 g, 33 mmol) was added and refluxed for 8 h. The solvent was evaporated under vacuum and product was obtained on purification through column chromatography on silica gel.
Reference: [1] Tetrahedron Letters, 2017, vol. 58, # 19, p. 1891 - 1894
  • 4
  • [ 623-33-6 ]
  • [ 95-92-1 ]
  • [ 29655-79-6 ]
Reference: [1] Journal of Heterocyclic Chemistry, 1995, vol. 32, # 6, p. 1693 - 1702
  • 5
  • [ 4755-77-5 ]
  • [ 29655-79-6 ]
Reference: [1] Patent: US2002/35115, 2002, A1,
  • 6
  • [ 64-17-5 ]
  • [ 144-62-7 ]
  • [ 56-40-6 ]
  • [ 29655-79-6 ]
Reference: [1] Bulletin of the Chemical Society of Japan, 1972, vol. 45, p. 1917 - 1918
  • 7
  • [ 29655-79-6 ]
  • [ 221136-66-9 ]
Reference: [1] Bioorganic and Medicinal Chemistry Letters, 2002, vol. 12, # 8, p. 1203 - 1208
[2] Synthetic Communications, 2000, vol. 30, # 17, p. 3171 - 3180
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