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[ CAS No. 1577-22-6 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
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Chemical Structure| 1577-22-6
Chemical Structure| 1577-22-6
Structure of 1577-22-6 * Storage: {[proInfo.prStorage]}

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Product Details of [ 1577-22-6 ]

CAS No. :1577-22-6 MDL No. :MFCD00046558
Formula : C6H10O2 Boiling Point : No data available
Linear Structure Formula :CH2CH(CH2)3C(O)OH InChI Key :XUDOZULIAWNMIU-UHFFFAOYSA-N
M.W : 114.14 Pubchem ID :15308
Synonyms :

Safety of [ 1577-22-6 ]

Signal Word:Danger Class:8
Precautionary Statements:P234-P260-P264-P280-P301+P330+P331-P303+P361+P353-P304+P340-P305+P351+P338-P310-P321-P363-P390-P405-P406-P501 UN#:3265
Hazard Statements:H290-H314 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 1577-22-6 ]

* 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.

  • Downstream synthetic route of [ 1577-22-6 ]

[ 1577-22-6 ] Synthesis Path-Downstream   1~3

  • 2
  • [ 105-60-2 ]
  • [ 7647-01-0 ]
  • [ 7732-18-5 ]
  • NaNO2 [ No CAS ]
  • [ 1577-22-6 ]
  • [ 4224-62-8 ]
  • 3
  • [ 1577-22-6 ]
  • C16H28O3 [ No CAS ]
  • [ 551-11-1 ]
YieldReaction ConditionsOperation in experiment
75% With (Z)-2-Butene; C37H40Cl2N2ORuS2; In tetrahydrofuran; at 22℃; under 7 Torr;Inert atmosphere; Glovebox; Sealed tube; General procedure: In a N2-filled glovebox, an oven-dried vial equipped with a magnetic stir bar is charged with the alkene substrates (1 :3 ratio), unpurified Z-2-butene (3) and a solution of the appropriate amount of catec -2 (WO 2014/201300) Ru-2 dissolved in THF. The reaction vessel is then sealed. The mixture is allowed to stir at 22 C for 4 h, after which the volatiles are removed in vacuo (typically, 100 torr for 2 mins).The flask containing the residue is then charged with a solution of the appropriate amount of Ru-2 in THF and the system is placed under 100 torr of vacuum. The resulting solution is allowed to stir for 8 h at 22 C, after which the reaction is quenched by the addition of wet (undistilled) diethyl ether and the volatiles were removed in vacuo. Purification may be performed by silica gel chromatography. [00124] The following examples show the effectiveness of the method using as internal olefin according to steps (X), (Y) or (V) Z-2-butene (3). For example, biologically active compounds such as prostaglandins may be prepared:
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