Home Cart Sign in  
Chemical Structure| 4909-95-9 Chemical Structure| 4909-95-9

Structure of 4909-95-9

Chemical Structure| 4909-95-9

*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 [ 4909-95-9 ]

CAS No. :4909-95-9
Formula : C10H11NO
M.W : 161.20
SMILES Code : N#CC1=CC(C)=C(O)C(CC)=C1
MDL No. :MFCD24713706

Safety of [ 4909-95-9 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302
Precautionary Statements:P280-P305+P351+P338

Application In Synthesis of [ 4909-95-9 ]

* 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 [ 4909-95-9 ]

[ 4909-95-9 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 4728-12-5 ]
  • [ 4909-95-9 ]
  • [ 1186605-95-7 ]
YieldReaction ConditionsOperation in experiment
With triphenylphosphine; diethylazodicarboxylate; In tetrahydrofuran; toluene; at 4 - 20℃; for 1.25h; To a solution of 3-ethyl-4-hydroxy-5-methyl-benzonitrile (480 mg, 2.98 mmol) in THF (10 mL), triphenylphosphine (1.17 g, 4.47 mmol) and (2,2-dimethyl-[1 ,3]dioxan-5-yl)-methanol (478 mg, 3.28 mmol) is added. The mixture is cooled to 4°C before DEAD (1.94 g, 4.47 mmol, 2.05 mL of a 40percent solution in toluene) is added. Stirring is continued at 4°C for 15 min, then at rt for 1 h. The solvent is removed in vacuo and the crude product is purified by CC on silica gel eluting with heptane:EA 9:1 to give 4-(2,2-dimethyl-[1 ,3]dioxan-5- ylmethoxy)-3-ethyl-5-methyl-benzonitrile (240 mg) as a yellow oil; LC-MS: tR = 1.04 min; <n="39"/>[M+ 1 +CH3CN]+ = 330.97. To a solution of this material (240 mg, 829 mumol) in methanol (5 ml_), hydroxylamine hydrochloride (86 mg, 1.24 mmol) and NaHCO3 (104 mg, 1.24 mmol) is added. The mixture is stirred at 600C for 5 h before it is diluted with EA and washed with water. The org. extract is dried over MgSO4, filtered, concentrated and dried to give the title compound (280 mg) as a pale yellow oil; LC-MS: tR = 0.72 min; [M+1 +CH3CN]+ = 323.01.
  • 2
  • [ 4728-12-5 ]
  • [ 4909-95-9 ]
  • [ 1150644-94-2 ]
 

Historical Records

Technical Information

Categories