Home Cart Sign in  
Chemical Structure| 10347-01-0 Chemical Structure| 10347-01-0

Structure of 10347-01-0

Chemical Structure| 10347-01-0

*Storage: {[sel_prStorage]}

*Shipping: {[sel_prShipping]}

,{[proInfo.pro_purity]}

4.5 *For Research Use Only !

{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]} Purity: {[proInfo.pro_purity]}

Change View

Size Price VIP Price

US Stock

Global Stock

In Stock
{[ item.pr_size ]} Inquiry {[ getRatePrice(item.pr_usd,item.pr_rate,item.mem_rate,item.pr_is_large_size_no_price, item.vip_usd) ]}

US Stock: ship in 0-1 business day
Global Stock: ship in 5-7 days

  • {[ item.pr_size ]}

In Stock

- +

Please Login or Create an Account to: See VIP prices and availability

US Stock: ship in 0-1 business day
Global Stock: ship in 2 weeks

  • 1-2 Day Shipping
  • High Quality
  • Technical Support
Product Citations

Alternative Products

Product Details of [ 10347-01-0 ]

CAS No. :10347-01-0
Formula : C12H20O2
M.W : 196.29
SMILES Code : OC12CC3(O)CC(C2)(C)CC(C3)(C)C1
MDL No. :MFCD00077198

Safety of [ 10347-01-0 ]

Application In Synthesis of [ 10347-01-0 ]

* 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 [ 10347-01-0 ]

[ 10347-01-0 ] Synthesis Path-Downstream   1~5

  • 1
  • [ 702-79-4 ]
  • [ 707-37-9 ]
  • [ 10347-01-0 ]
YieldReaction ConditionsOperation in experiment
7.3%Chromat.; 68.4%Chromat. With N-hydroxyphthalimide; cobalt(II) acetate; ozone; acetic acid; at 38 - 46℃; for 8h; In a 100 mL round bottom flask, 12.9 g of DMA, 0.12 g of cobalt (II) acetate tetrahydrate, 1.02 g of NHPI and 52.45 g of acetic acid were charged, a stirrer was placed, and stirred Was carried out.The flask was equipped with a thermometer and a glass gas introduction pipe, and the gas was passed through a cooling pipe, passed through a water trap, an ozone decomposition column, and exhausted.Heating to 40 C. was carried out and a reaction was carried out while maintaining the temperature in the range of 38 to 46 C. while blowing ozone-containing gas containing ozone equivalent to 4.9 g / h through a glass tube.A small amount of sampling was carried out at the time when 2, 4, 6, 8 hours passed since the start of the reaction, and the reaction was continued while tracking the composition change by GC-FID analysis.After 8 hours, DMAO was 7.3 area% by area percentage method, DMAD was 68.4 area%, and DMA was not detected with respect to the sum of peak areas other than acetic acid used for solvent.
50.1%Chromat.; 21%Chromat. With ozone; acetic acid; at 10 - 20℃; for 15h; The same procedure as in Comparative Example 1 was carried out except that 130 mL of acetic acid containing 50% of water was charged as a solvent and the reaction was carried out while maintaining the reaction temperature in the range of 10 to 20 C.After 5, 10, and 15 hours from the start of the reaction, a small amount of sampling was carried out and the reaction was continued while tracking the composition change by GC-FID analysis.When 15 hours passed, DMA was 0.7 area% by area percentage method, DMAO was 50.1 area%, DMAD was 21.0 area%, with respect to the sum of peak areas other than acetic acid used for the solvent.
  • 2
  • [ 702-79-4 ]
  • [ 33794-98-8 ]
  • [ 707-37-9 ]
  • [ 10347-01-0 ]
  • 3
  • [ 524-38-9 ]
  • Co(AA)2 [ No CAS ]
  • [ 702-79-4 ]
  • [ 707-37-9 ]
  • [ 10347-01-0 ]
YieldReaction ConditionsOperation in experiment
58% With acetic acid; Example D8 A mixture of 1.64 grams (10 millimoles) of <strong>[702-79-4]1,3-dimethyladamantane</strong>, 0.13 gram (0.8 millimole) of N-hydroxyphthalimide, 0.015 gram (0.06 millimole) of Co(AA)2 and 10 milliliters of acetic acid was stirred under oxygen atmosphere at a temperature of 70 C. for six hours. As a result, with a transformation rate for <strong>[702-79-4]1,3-dimethyladamantane</strong> of 99%, 1-hydroxy-3,5-dimethyladamantane (yield 39%), and 1,3-dihydroxy-5,7-dimethyladamantane (yield 58%) were obtained. The selectivity for the alcohols was 97%.
  • 4
  • [ 702-79-4 ]
  • [ 10347-01-0 ]
YieldReaction ConditionsOperation in experiment
82.7%Chromat. With 1-hydroxy-pyrrolidine-2,5-dione; cobalt(II) acetate; ozone; acetic acid; at 31℃; for 6h; In a 20 L columnar separable flask, 1881 g of DMA, 17.49 g of cobalt (II) acetate tetrahydrate, 106.39 g of NHSI and 8182 g of acetic acid were charged and stirred using a mechanical stirrer.The flask was equipped with a thermometer and a glass gas introduction pipe, and the gas was passed through a cooling pipe, passed through a water trap, an ozone decomposition column, and exhausted.Cooling was carried out in a 20 C. water bath and reaction was carried out while maintaining the temperature in the range of 20 to 35 C. while blowing ozone-containing gas containing ozone equivalent to 119.5 g / h through the glass tube.A small amount of sampling was carried out after 2, 4 and 6 hours from the start of the reaction, and the reaction was continued while tracking the composition change by GCFID analysis.After 6 hours, DMAO was 1.9 area% by area percentage method, DMAD was 82.7 area%, and DMA was not detected, with respect to the sum of the peak areas other than acetic acid used for the solvent.The blowing of ozone was stopped, 437 mL of a 16.7% by weight sodium sulfite aqueous solution was added, and the mixture was stirred. At this point, the total reaction weight is 11.852 kg.As a result of quantitative determination by GC, the DMAO was 0.25% by weight and the DMAD was 11.02% by weight. When the conversion and the selectivity were calculated, the conversion of DMA was 100%, the conversion of DMAO Was 1.45% and the selectivity of DMAD was 58.1%.
  • 5
  • [ 702-79-4 ]
  • [ 707-37-9 ]
  • [ 6663-13-4 ]
  • [ 10347-01-0 ]
 

Historical Records

Technical Information

Categories