Select Region or Location
Americas
  • Argentina
  • Brazil
  • Canada
  • Mexico
  • United States
  • Other Americas
Europe
  • Austria
  • Belgium
  • Bulgaria
  • Croatia/Hrvatska
  • Cyprus
  • Czech Republic
  • Denmark
  • Estonia
  • Finland
  • France
  • Germany
  • Greece
  • Hungary
  • Ireland
  • Italy
  • Latvia
  • Liechtenstein
  • Lithuania
  • Luxembourg
  • Malta
  • Netherlands
  • Norway
  • Poland
  • Portugal
  • Romania
  • Slovak Republic
  • Slovenia
  • Spain
  • Sweden
  • Switzerland
  • Turkey
  • United Kingdom
  • Other Europe
Asia Pacific
  • Australia
  • China
  • India
  • Indonesia
  • Japan
  • Korea, Republic of
  • Malaysia
  • New Zealand
  • Philippines
  • Singapore
  • Thailand
  • Vietnam
  • Other Asia Pacific
Africa And Middle East
  • Egypt
  • Israel
  • Other Africa And Middle East
USD
Home Cart Sign in  
Chemical Structure| 190898-86-3 Chemical Structure| 190898-86-3

Structure of 190898-86-3

Chemical Structure| 190898-86-3

*Storage: {[sel_prStorage]}

*Shipping: {[sel_prShipping]}

,{[proInfo.pro_purity]}

4.5 *For Research Use Only! Not for Human Use. We Do Not Sell to Patients.

{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]} Purity: {[proInfo.pro_purity]}

Change View

Size Price VIP Price

DE Stock

US Stock

Asia Stock

Global Stock

In Stock
{[ item.pr_size ]}{[ size_append_text(item.pr_size, proInfo.prAm, 'list') ]} Inquiry {[ getRatePrice(item.pr_usd,item.pr_rate,item.mem_rate,item.pr_is_large_size_no_price, item.vip_usd) ]}

  • {[ item.pr_size ]}
    {[ size_append_text(item.pr_size, proInfo.prAm, 'list') ]}

In Stock

- +

Please Login or Create an Account to: See VIP prices and availability

  • 1-2 Day Shipping
  • High Quality
  • Technical Support
Product Citations

Alternative Products

Product Details of [ 190898-86-3 ]

CAS No. :190898-86-3
Formula : C16H11BrClNO
M.W : 348.62
SMILES Code : COC1=NC2=CC=C(Br)C=C2C(C3=CC=CC(Cl)=C3)=C1
English Name :6-Bromo-4-(3-chlorophenyl)-2-methoxyquinoline
MDL No. :MFCD28502381

Safety of [ 190898-86-3 ]

Application In Synthesis of [ 190898-86-3 ]

* 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 [ 190898-86-3 ]

[ 190898-86-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 190898-86-3 ]
  • [ 192185-72-1 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 7 steps 1.1: n-butyllithium / tetrahydrofuran / 0.5 h / -70 °C 1.2: 75 percent / tetrahydrofuran / 0.5 h / -70 °C 2.1: 80 percent / aq. HCl; MeOH / 72 h / 60 °C 3.1: 75 percent / benzyltriethylammonium chloride; aq. NaOH / tetrahydrofuran / 16 h / 20 °C 4.1: n-butyllithium; triethylsilyl chloride / tetrahydrofuran; hexane / -78 - 20 °C 4.2: tetrahydrofuran; hexane / 1 h / -78 °C 4.3: 52 percent / water / tetrahydrofuran; hexane / -50 °C 5.1: 3.49 g / thionyl chloride / 40 °C 6.1: ammonia; methanol / 20 h / 22 °C 7.1: L-(-)-dibenzoyltartaric acid monohydrate / acetone / 22 h / 22 °C 7.2: aq. ammonium hydroxide / ethanol / 2 h / 25 - 80 °C
Multi-step reaction with 6 steps 1.1: n-butyllithium / tetrahydrofuran / 0.5 h / -70 °C 1.2: 75 percent / tetrahydrofuran / 0.5 h / -70 °C 2.1: 80 percent / aq. HCl; MeOH / 72 h / 60 °C 3.1: 75 percent / benzyltriethylammonium chloride; aq. NaOH / tetrahydrofuran / 16 h / 20 °C 4.1: n-butyllithium; triethylsilyl chloride / tetrahydrofuran; hexane / -78 - 20 °C 4.2: tetrahydrofuran; hexane / 1 h / -78 °C 4.3: 52 percent / water / tetrahydrofuran; hexane / -50 °C 5.1: 3.49 g / thionyl chloride / 40 °C 6.1: NH4OH / tetrahydrofuran / 0.5 h / 80 °C 6.2: Chiracel OD
Multi-step reaction with 7 steps 1.1: n-butyllithium / tetrahydrofuran / 0.5 h / -70 °C 1.2: 75 percent / tetrahydrofuran / 0.5 h / -70 °C 2.1: 80 percent / aq. HCl; MeOH / 72 h / 60 °C 3.1: 75 percent / benzyltriethylammonium chloride; aq. NaOH / tetrahydrofuran / 16 h / 20 °C 4.1: n-hexyllithium; triisobutylsilyl chloride / tetrahydrofuran; hexane / -15 - 0 °C 4.2: tetrahydrofuran; hexane / 0.25 h / -5 - 0 °C 4.3: 75.6 percent / aq. acetic acid / tetrahydrofuran; hexane / 2 h / 40 °C 5.1: 3.49 g / thionyl chloride / 40 °C 6.1: ammonia; methanol / 20 h / 22 °C 7.1: L-(-)-dibenzoyltartaric acid monohydrate / acetone / 22 h / 22 °C 7.2: aq. ammonium hydroxide / ethanol / 2 h / 25 - 80 °C
Multi-step reaction with 6 steps 1.1: n-butyllithium / tetrahydrofuran / 0.5 h / -70 °C 1.2: 75 percent / tetrahydrofuran / 0.5 h / -70 °C 2.1: 80 percent / aq. HCl; MeOH / 72 h / 60 °C 3.1: 75 percent / benzyltriethylammonium chloride; aq. NaOH / tetrahydrofuran / 16 h / 20 °C 4.1: n-hexyllithium; triisobutylsilyl chloride / tetrahydrofuran; hexane / -15 - 0 °C 4.2: tetrahydrofuran; hexane / 0.25 h / -5 - 0 °C 4.3: 75.6 percent / aq. acetic acid / tetrahydrofuran; hexane / 2 h / 40 °C 5.1: 3.49 g / thionyl chloride / 40 °C 6.1: NH4OH / tetrahydrofuran / 0.5 h / 80 °C 6.2: Chiracel OD

 

Historical Records