成人免费xx,国产又黄又湿又刺激不卡网站,成人性视频app菠萝网站,色天天天天

Home Cart Sign in  
Chemical Structure| 10192-85-5 Chemical Structure| 10192-85-5

Structure of 10192-85-5

Chemical Structure| 10192-85-5

*Storage: {[sel_prStorage]}

*Shipping: {[sel_prShipping]}

{[proInfo.proName]}

CAS No.: 10192-85-5

,{[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 2 weeks

  • {[ 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 [ 10192-85-5 ]

CAS No. :10192-85-5
Formula : C3H3KO2
M.W : 110.15
SMILES Code : C=CC([O-])=O.[K+]
MDL No. :MFCD00067206
InChI Key :ZUBIJGNKOJGGCI-UHFFFAOYSA-M
Pubchem ID :4429391

Safety of [ 10192-85-5 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P261-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P321-P332+P313-P337+P313-P362-P403+P233-P405-P501

Application In Synthesis of [ 10192-85-5 ]

* 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 [ 10192-85-5 ]

[ 10192-85-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 2043-55-2 ]
  • [ 10192-85-5 ]
  • [ 52591-27-2 ]
  • [ 19430-93-4 ]
  • [ 2043-47-2 ]
YieldReaction ConditionsOperation in experiment
With 10H-phenothiazine; In tert-butyl alcohol; at 160℃; for 6h; Into a pressure resistant autoclave (0.5 liter) equipped with stirring vanes (disk turbine), FI, potassium (meth)acrylate, PTZ and BuOH were charged in the amounts (unit: mol) as shown in Table 1, and an ester-forming reaction was carried out under the reaction conditions shown in Table 1 to obtain a reaction mixture. The conversion and selectivity of the reaction are shown in Table 1.
 

Historical Records

Technical Information

Categories