Home Cart Sign in  
Chemical Structure| 875781-62-7 Chemical Structure| 875781-62-7

Structure of 875781-62-7

Chemical Structure| 875781-62-7

*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 [ 875781-62-7 ]

CAS No. :875781-62-7
Formula : C8H10BNO4
M.W : 194.98
SMILES Code : O=C(C1=CN=CC(B(O)O)=C1)OCC
MDL No. :MFCD09952043
InChI Key :ANWGKOKCTGJGCD-UHFFFAOYSA-N
Pubchem ID :55265795

Safety of [ 875781-62-7 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319
Precautionary Statements:P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313

Application In Synthesis of [ 875781-62-7 ]

* 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 [ 875781-62-7 ]

[ 875781-62-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 875781-62-7 ]
  • [ 71831-21-5 ]
  • ethyl 5-(4-(hydroxymethyl)benzyl)nicotinate [ No CAS ]
YieldReaction ConditionsOperation in experiment
37% With tetrakis(triphenylphosphine) palladium(0); sodium carbonate; In 1,4-dioxane; water; at 85℃;Inert atmosphere; A mixture of <strong>[71831-21-5](4-(bromomethyl)phenyl)methanol</strong> (200 mg, 1.0 mmol), (5-(ethoxycarbonyl)pyridin-3- yl)boronic acid (195 mg, 1.0 mmol), Pd(PPh4)3 (116 mg, 0.1 mmol), and Na2C03 (318 mg, 3.0 mmol) in 1,4- dioxane (10 mL) and H2O (2 mL) was heated at 85 °C overnight under N2. The mixture was diluted with water (100 mL) and extracted with EA (50 mL X 3). The combined organic layers were dried over anhydrous sodium sulfate and concentrated. The residue was purified via prep-HPLC to affored ethyl 5-(4- (hydroxymethyl)benzyl)
 

Historical Records

Technical Information

Categories