Home Cart Sign in  
Chemical Structure| 1602682-09-6 Chemical Structure| 1602682-09-6

Structure of 1602682-09-6

Chemical Structure| 1602682-09-6

*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 [ 1602682-09-6 ]

CAS No. :1602682-09-6
Formula : C9H12BrNO
M.W : 230.10
SMILES Code : CC(C1=CC=CC(Br)=N1)(OC)C
MDL No. :MFCD28674595

Safety of [ 1602682-09-6 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P330-P332+P313-P337+P313-P362-P403+P233-P405-P501

Application In Synthesis of [ 1602682-09-6 ]

* 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 [ 1602682-09-6 ]

[ 1602682-09-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 638218-78-7 ]
  • [ 74-88-4 ]
  • [ 1602682-09-6 ]
YieldReaction ConditionsOperation in experiment
81% With sodium hydride; In tetrahydrofuran; mineral oil; at 20℃; Step 1 2-Bromo-6-(2-methoxypropan-2-yl)pyridine A dry flask fitted with a stir bar and septum was charged with 2-(6-bromopyridin-2-yl)propan-2- ol (1.66 g, 7.68 mmol), Mel (3.27 g, 1.44 mL, 23.0 mmol) and THF (40 mL). NaH (60% in mineral oil, 922 mg, 23.0 mmol) was added portion wise over 10 min and the reaction then stirred at room temperature overnight. Saturated aqueous ammonium chloride (20 mL) was added and the mixture extracted with dichloro methane (3 x 75 mL). The combined organic extracts were dried over magnesium sulfate, concentrated in vacuo, and purified by a chromatography (silica gel 50 muiotaeta, 80g, Analogix, eluting with dichloromethane) to give 2- bromo-6-(2-methoxypropan-2-yl)pyridine (1.473 g, 81 %) as a clear liquid1 NMR (CHLOROFORM-d) delta: 7.49 - 7.57 (m, 2H), 7.34 (dd, J = 6.6, 2.1 Hz, 1H), 3.19 (s, 3H), 1.54 (s, 6H); . MS (EI/CI) m/z: 230.0, 232.0 [M + H].
 

Historical Records