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[ CAS No. 646-07-1 ] {[proInfo.proName]}

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Chemical Structure| 646-07-1
Chemical Structure| 646-07-1
Structure of 646-07-1 * Storage: {[proInfo.prStorage]}

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Product Details of [ 646-07-1 ]

CAS No. :646-07-1 MDL No. :MFCD00002803
Formula : C6H12O2 Boiling Point : -
Linear Structure Formula :HOOCCH2CH2CH(CH3)2 InChI Key :FGKJLKRYENPLQH-UHFFFAOYSA-N
M.W : 116.16 Pubchem ID :12587
Synonyms :
Isocaproic Acid

Safety of [ 646-07-1 ]

Signal Word:Danger Class:6.1
Precautionary Statements:P280-P312 UN#:2810
Hazard Statements:H311-H315 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 646-07-1 ]

* 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 [ 646-07-1 ]

[ 646-07-1 ] Synthesis Path-Downstream   1~10

  • 1
  • [ 3123-97-5 ]
  • [ 646-07-1 ]
YieldReaction ConditionsOperation in experiment
95% With palladium 10% on activated carbon; W(OTf)6; hydrogen; at 100℃; under 760.051 Torr; for 12h; Specific methods are as follows: propiolactone was added (0.36g, 5mmol), palladium on carbon (10%, 26.5mg, 0.025mmol, 0.5mol%) in the reactor and W (OTf)6(107.8mg, 0.1mmol, 2mol%). A hydrogen balloon connected to the top of the reactor, and the reactor was purged with hydrogen gas atmosphere. Hydrogen atmosphere at normal pressure, the reaction was stirred at 135 deg.] C after 12h, detected by gas, gamma- valerolactone complete conversion of starting material, and only n-valeric acid. The method carried out as follows completion of the hydrogenation reaction of the ring-opening reaction system separation, to obtain the desired product n-valeric acid: The reaction was completed reaction mixture was dissolved with methylene chloride, filtered to remove the palladium on carbon catalyst and W (OTf)699% yield measured propionic acid, purity of the product was 99%. NMR data for the product using the embodiment of the present invention is the NMR identified the product as follows:The specific reaction procedure and operation method were the same as in Example 27 except that the reaction temperature was changed to 100 C, the yield was 95%, and the purity of the product was 99%. The product was subjected to nuclear magnetic identification using the manner described in the present invention, and the NMR data of the product were as follows:
  • 4
  • [ 3123-97-5 ]
  • [ 10034-85-2 ]
  • red phosphorus [ No CAS ]
  • [ 646-07-1 ]
  • 5
  • [ 513-35-9 ]
  • [ 7732-18-5 ]
  • [ 10034-85-2 ]
  • carbon monoxide [ No CAS ]
  • nickel acetate [ No CAS ]
  • [ 14287-61-7 ]
  • [ 105-43-1 ]
  • [ 646-07-1 ]
  • 6
  • [ 646-07-1 ]
  • potassium permanganate [ No CAS ]
  • alkali [ No CAS ]
  • [ 3123-97-5 ]
  • 7
  • [ 646-07-1 ]
  • deuteriosulfuric acid [ No CAS ]
  • [ 15262-86-9 ]
  • 10
  • [ 646-07-1 ]
  • [ 3123-97-5 ]
  • [ 23327-19-7 ]
  • [ 74397-28-7 ]
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