Home Cart Sign in  
Chemical Structure| 771464-30-3 Chemical Structure| 771464-30-3

Structure of 771464-30-3

Chemical Structure| 771464-30-3

*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 [ 771464-30-3 ]

CAS No. :771464-30-3
Formula : C11H8ClNO3
M.W : 237.64
SMILES Code : O=C(O)C1C=C2C(N=CC=C2Cl)=CC=1OC
MDL No. :MFCD25541904
InChI Key :NJNCUNAOBIJAQR-UHFFFAOYSA-N
Pubchem ID :22988092

Safety of [ 771464-30-3 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of [ 771464-30-3 ]

* 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 [ 771464-30-3 ]

[ 771464-30-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 771464-30-3 ]
  • [ 1258500-63-8 ]
  • [ 19499-93-5 ]
  • [ 417723-77-4 ]
YieldReaction ConditionsOperation in experiment
In tetrahydrofuran; methanol; Production Example 490-1 4-(6-Carbamoyl-7-methoxy-4-quinolyl)oxy-2,3-dimethylphenylamine The title compound (840 mg) was obtained from 7-methoxy-4-chloroquinoline-6-carboxyamide (890 mg) and <strong>[19499-93-5]4-nitro-2,3-dimethylphenol</strong> (940 mg), in the same manner as Production Example 7. Next, 6-carbamoyl-4-(2,3-dimethyl-4-nitrophenoxy)-7-methoxyquinoline (840 mg) was dissolved in tetrahydrofuran (25 ml) and methanol (25 ml), and the solution was subjected to catalytic reduction with palladium-carbon (840 mg) for 10 hours under a hydrogen atmosphere to obtain the title compound (639 mg). 1H-NMR (DMSO-d6) delta (ppm) 1.92 (3H, s), 2.02 (3H, s) 4.00 (3H, s), 4.82-4.88 (2H, m), 6.22 (1H, d, J=5.2 Hz), 6.60 (1H, d, J=8.4 Hz), 6.75 (1H, d, J=8.4 Hz), 7.471H, s), 7.71 (1H, brs), 7.84 (1H, brs), 8.57 (1H, d, J=5.2 Hz), 8.70 (1H, s).
 

Historical Records

Technical Information

Categories