Home Cart Sign in  
Chemical Structure| 30236-02-3 Chemical Structure| 30236-02-3

Structure of 30236-02-3

Chemical Structure| 30236-02-3

*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 [ 30236-02-3 ]

CAS No. :30236-02-3
Formula : C12H9BrO2
M.W : 265.10
SMILES Code : O=C(O)C1=C2C=CC=CC2=C(CBr)C=C1
MDL No. :MFCD00228229

Safety of [ 30236-02-3 ]

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

Application In Synthesis of [ 30236-02-3 ]

* 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 [ 30236-02-3 ]

[ 30236-02-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 4488-40-8 ]
  • [ 30236-02-3 ]
YieldReaction ConditionsOperation in experiment
80% With N-Bromosuccinimide; azobisisobutyronitrile; In tetrachloromethane; ethyl acetate; 4-Bromomethylnaphthoic Acid: A mixture of 4-methylnaphthoic acid (10 g, 54 mmol), N-bromosuccinimide (10 g, 56 mmol) and AIBN (100 mg) in CCl4 (250 mL) was refluxed for 3 hr. The reaction mixture was concentrated and dissolved in ethyl acetate. The organic layer was washed with water, brine and dried over MgSO4. Evaporation of the solvent gave the desired product (16 g, 80%). 1H NMR (DMSO-D6): delta 5.24 (s, 2H), 7.73 (m, 3H), 8.03 (d, 1H), 8.28 (d, 1H), 8.86 (d, 1H), 13.29 (brd s, 1H).
71% With N-Bromosuccinimide;1,1'-azobis(1-cyanocyclohexanenitrile); In 1,2-dichloro-ethane; at 80℃; for 4h; Step A. The preparation of 4-(bromomethy I)-I -naphthoic acid; <n="45"/>4-MethyInaphthoic acid (1.05 g, 5.66 mmol), N-bromosuccinimide (1.01 g) and 1,1'- azobis(cyclohexane-carbonitrile) (50 mg, catalytic amount) were placed in a round- bottomed flask. 1,2-Dichloroethane (40 ml) was added and the mixture heated at 8O0C for 4 h. Volatiles were evaporated tinder vacuum. The residue was dissolved in a mixture of ethyl acetate and water, phases were separated and the organic phase dried over calcium chloride. After evaporation of solvent, the product was obtained as a white solid (1.07 g, 71%). 1H- NMR (400 MHz, CD3OD) delta: 5:08 (s, 2 H); 7.51 - 7.81 (m, 3 H); 8.10 (d, J=7.42 Hz, 1 H); 8.18 - 8.39 (m, 1 H); 8.85 - 9.09 (m, 1 H).
With N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile); In tetrachloromethane; for 2h;Reflux; 4-methylnaphthalen-l-carboxylic acid (5 g), N-bromosuccinimide (5.7 g) and 2,2'- azobisisobutyronitrile (0.2 g) were suspended in carbon tetrachloride (50 ml) and then heated to <n="65"/>reflux for 2 hours. The mixture was returned to room temperature and added a 15% aqueous solution of citric acid (20 ml), and stirred for some time. Resulting crystals were filtered and washed with the 15% aqueous solution of citric acid (20 ml), and then dried, to obtain 4- (bromomethyl)naphthalen-l-carboxylic acid (7 g).IH-NMR (acetone-d6) delta: 5.19 (2H, s), 7.69-7.76 (3H, m), 8.23-8.29 (2H, m), 9.04-9.06 (IH, m)
 

Historical Records