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| 325685-59-4 Chemical Structure| 325685-59-4

Structure of 325685-59-4

Chemical Structure| 325685-59-4

*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 [ 325685-59-4 ]

CAS No. :325685-59-4
Formula : C12H11ClN2O
M.W : 234.68
SMILES Code : COCC1=CC(Cl)=NC(C2=CC=CC=C2)=N1
English Name :4-Chloro-6-(methoxymethyl)-2-phenylpyrimidine
MDL No. :MFCD00794769
InChI Key :GSSSCZAOXFZADM-UHFFFAOYSA-N
Pubchem ID :2763927

Safety of [ 325685-59-4 ]

Application In Synthesis of [ 325685-59-4 ]

* 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 [ 325685-59-4 ]

[ 325685-59-4 ] Synthesis Path-Downstream   1~8

  • 1
  • [ 127958-19-4 ]
  • [ 325685-59-4 ]
YieldReaction ConditionsOperation in experiment
29.0 g With trichlorophosphate for 3h; Heating;
  • 2
  • [ 97674-02-7 ]
  • [ 325685-59-4 ]
  • [ CAS Unavailable ]
YieldReaction ConditionsOperation in experiment
Stage #1: tributyl(1-ethoxyvinyl)stannane; 4-chloro-6-methoxymethyl-2-phenylpyrimidine In N,N-dimethyl-formamide at 80℃; for 24h; Stage #2: With potassium fluoride In diethyl ether; N,N-dimethyl-formamide at 20℃; for 0.666667h; Further stages.;
  • 3
  • [ 325685-59-4 ]
  • [ 325685-75-4 ]
YieldReaction ConditionsOperation in experiment
100% With boron tribromide In dichloromethane at 0℃; for 0.5h; Inert atmosphere;
99% Stage #1: 4-chloro-6-methoxymethyl-2-phenylpyrimidine With boron tribromide In dichloromethane at -12 - 0℃; for 3h; Stage #2: With water In diethyl ether; dichloromethane at 20℃; for 2h; Further stages.;
Stage #1: 4-chloro-6-methoxymethyl-2-phenylpyrimidine With boron tribromide In DCM at 0℃; for 0.5h; Inert atmosphere; Stage #2: With water; sodium hydroxide In DCM; diethyl ether 1.5 1.5. (6-chloro-2-phenyl-pyrimidin-4-yl)-methanol A solution of BBr3 (1.83 ml) in DCM (25 ml) was syringed into a solution of intermediate 1.4 (4.17 g) in DCM (90 ml) under argon at 0° C. After 30 min at 0° C., the reaction was complete. It was quenched by the addition of Et2O (100 ml), water (100 ml) and 1M NaOH solution (100 ml). After 1 h stirring at RT, the mixture was extracted with DCM, and the org. layers were washed with water, dried (Na2SO4) and evaporated. The resulting oil crushed out, and the solid obtained was washed with Hept. After HV drying, 3.29 g of a beige powder were obtained. LC-MS: tR=0.88 min; [M+H]+: 221.26.
Stage #1: 4-chloro-6-methoxymethyl-2-phenylpyrimidine With boron tribromide In dichloromethane at 0℃; for 0.5h; Inert atmosphere; Stage #2: With water; sodium hydroxide In diethyl ether; dichloromethane at 20℃; for 1h; 1.1.5 1.5. (6-chloro-2-phenyl-pyrimidin-4-yl)-methanol; A solution of BBr3 (1.83 ml) in DCM (25 ml) was syringed into a solution of intermediate 1.4 (4.17 g) in DCM (90 ml) under argon at 0°C. After 30 min at 0°C, the reaction was complete. It was quenched by the addition of Et2O (100 ml), water (100 ml) and 1M NaOH solution (100 ml). After 1 h stirring at RT, the mixture was extracted with DCM, and the org. layers were washed with water, dried (Na2SO4 and evaporated. The resulting oil crushed out, and the solid obtained was washed with Hept. After HV drying, 3.29 g of a beige powder were obtained. LC-MS: tR = 0.88 min; [M+H]+: 221.26.
With boron tribromide In dichloromethane at 0℃;

  • 4
  • [ 13737-05-8 ]
  • [ 325685-59-4 ]
  • [ 922726-27-0 ]
YieldReaction ConditionsOperation in experiment
70% With tetrakis(triphenylphosphine) palladium(0) In toluene for 12h; Heating;
  • 5
  • [ 60-34-4 ]
  • [ 325685-59-4 ]
  • [ 922726-19-0 ]
YieldReaction ConditionsOperation in experiment
80% In ethanol for 48h; Heating;
  • 6
  • [ 183368-58-3 ]
  • [ 325685-59-4 ]
  • [ 922726-28-1 ]
YieldReaction ConditionsOperation in experiment
61% With tetrakis(triphenylphosphine) palladium(0) In toluene for 12h; Heating;
  • 7
  • [ 325685-59-4 ]
  • [ 922726-32-7 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 3 steps 1: 70 percent / Pd(PPh3)4 / toluene / 12 h / Heating 2: BBr3 / CH2Cl2 / 16 h / 25 °C 3: 12 mg / Dess-Martin reagent / CH2Cl2 / 6 h
  • 8
  • [ 325685-59-4 ]
  • [ 922726-29-2 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1: 70 percent / Pd(PPh3)4 / toluene / 12 h / Heating 2: BBr3 / CH2Cl2 / 16 h / 25 °C
 

Historical Records

Technical Information

Categories