Home Cart Sign in  
Chemical Structure| 4393-06-0 Chemical Structure| 4393-06-0
Chemical Structure| 4393-06-0

*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 1-Phenylprop-2-en-1-ol

CAS No. :4393-06-0
Formula : C9H10O
M.W : 134.18
SMILES Code : C=CC(C1=CC=CC=C1)O
MDL No. :MFCD00093987
InChI Key :MHHJQVRGRPHIMR-UHFFFAOYSA-N
Pubchem ID :92986

Safety of 1-Phenylprop-2-en-1-ol

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of 1-Phenylprop-2-en-1-ol

* 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 [ 4393-06-0 ]

[ 4393-06-0 ] Synthesis Path-Downstream   1~8

  • 1
  • [ 51738-07-9 ]
  • [ 4393-06-0 ]
  • [ 1251839-60-7 ]
  • 2
  • [ 221044-05-9 ]
  • [ 4393-06-0 ]
  • [ 1446415-22-0 ]
YieldReaction ConditionsOperation in experiment
87% With silver hexafluoroantimonate; at 20℃; for 24h; To the polyethylene glycol-400 catalyst system obtained in Example 13 was added 1 mmol of N-pyrimidine indole and 2 mmol of 1-phenylpropen-1-ol, and the mixture was stirred at room temperature for 24 hours. The progress of the reaction was monitored by TLC. After completion, add ether to extract three times. The obtained polyethylene glycol-400 catalytic system was reused. It was put into the next experiment. The ether solution was combined and concentrated, and separated by column chromatography to obtain 285 mg of light yellow oily liquid with a yield of 87. %, the structural formula of the resulting product is as follows, the resulting polyethylene glycol-400 catalytic system is reused and put into the next experiment:
70% With silver hexafluoroantimonate; dichloro(pentamethylcyclopentadienyl)rhodium (III) dimer; In water; at 80℃; for 12h;Schlenk technique; Green chemistry; General procedure: Heterocycles 1 (0.2mmol, 1.0 equiv), allylic alcohols 2 (0.4 mmol, 2.0 equiv), [Cp*RhCl2]2 (2.5mol %), AgSbF6 (0.02mmol, 10mol %) and H2O (2mL) were charged into a Schlenk tube under air. The reaction mixture was stirred for 12hat 80C. After the reaction was complete, the mixture was extracted with CH2Cl2 three times. The combined organic layer was dried with anhydrous Na2SO4 and evaporated in vacuum. The crude product was purified by flash chromatography on silica gel using hexane/ethyl acetate as the eluent to give the pure product 3.
  • 4
  • [ 4393-06-0 ]
  • [ 1565-74-8 ]
  • [ 613-87-6 ]
  • [ 93-55-0 ]
YieldReaction ConditionsOperation in experiment
66% With C34H41ClFePRhS; hydrogen; sodium methylate; In tetrahydrofuran; at 82℃; under 22502.3 Torr; for 16h;Autoclave; Inert atmosphere; General procedure: A solution containing 6.4 × 10-3mmol of precatalyst and0.13 mmol of substrate (20 equiv.) in 2 mL of THF was transferred into a 5 mL glass vial which was then placed under argon into a stainless steel autoclave equipped with a magnetic stirring bar. The reaction vessel was pressurized with H2 to 30 bar and stirred for the desired time at room temperature. Then pressure was released andthe reaction vessel was stirred for the desired time at controlledtemperature under a dihydrogen atmosphere at 1 bar. Alterna-tively, after venting the H2pressure used for the catalyst activation,the residual H2was purged with argon by continuous flushingbefore continuing the reaction. The pure products were obtainedby chromatography of the reaction mixture on silica gel using dichloromethane as eluent and then analyzed by NMR spectrosopyand chiral GC for the determination of the yields and enantiomeric excesses.
  • 5
  • [ 201230-82-2 ]
  • [ 4393-06-0 ]
  • [ 5460-32-2 ]
  • [ 67756-25-6 ]
  • 6
  • [ 201230-82-2 ]
  • [ 4393-06-0 ]
  • [ 75676-72-1 ]
  • C17H15ClO3 [ No CAS ]
  • 8
  • [ 4393-06-0 ]
  • [ 101349-12-6 ]
  • C19H18FNO [ No CAS ]
 

Historical Records

Technical Information

Categories