*Storage: {[sel_prStorage]}
*Shipping: {[sel_prShipping]}
The BI-3802 was designed by Boehringer Ingelheim and could be obtained free of charge through the Boehringer Ingelheim open innovation portal opnMe.com, associated with its negative control.
4.5
*For Research Use Only! Not for Human Use. We Do Not Sell to Patients.
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, 1,1,item.pr_is_large_size_no_price, item.pr_usd) ]} {[ getRatePrice(item.pr_usd,item.pr_rate,1,item.pr_is_large_size_no_price, item.discount_usd) ]} {[ getRatePrice(item.pr_usd, 1,1,item.pr_is_large_size_no_price, item.pr_usd) ]} |
Inquiry {[ getRatePrice(item.pr_usd,item.pr_rate,item.mem_rate,item.pr_is_large_size_no_price, item.vip_usd) ]} | {[ item.p_spot_brand_remark ]} 1-2 weeks {[ item.pr_usastock ]} In Stock Inquiry - | {[ item.p_spot_brand_remark ]} 1-2 weeks {[ item.pr_chinastock ]} {[ item.pr_remark ]} In Stock Inquiry - | Login - + |
Please Login or Create an Account to: See VIP prices and availability
Asia Stock: Ship in 3-5 business days
EU Stock: ship in 0-1 business day
Global Stock: ship in 7-10 days
US Stock: ship in 0-1 business day
Global Stock: ship in 5-7 days
{[ item.p_spot_brand_remark ]}
1-2weeks
Inquiry
Inquiry
{[ getRatePrice(item.pr_usd,item.pr_rate,item.mem_rate,item.pr_is_large_size_no_price, item.vip_usd) ]}
{[ getRatePrice(item.pr_usd, 1,1,item.pr_is_large_size_no_price, item.pr_usd) ]}
{[ getRatePrice(item.pr_usd,1,item.mem_rate,item.pr_is_large_size_no_price, item.pr_usd) ]}
{[ item.p_spot_brand_remark ]}
1-2weeks
Inquiry
Inquiry
{[ getRatePrice(item.pr_usd,item.pr_rate,1,item.pr_is_large_size_no_price, item.vip_usd) ]}
{[ getRatePrice(item.pr_usd, 1,1,item.pr_is_large_size_no_price, item.pr_usd) ]}
{[ getRatePrice(item.pr_usd, 1,1,item.pr_is_large_size_no_price, item.pr_usd) ]}
In Stock
- +
Please Login or Create an Account to: See VIP prices and availability
Asia Stock: Ship in 3-5 business days
EU Stock: ship in 0-1 business day
Global Stock: ship in 7-10 days
US Stock: ship in 0-1 business day
Global Stock: ship in 5-7 days
Search for reports by entering the product batch number.
Batch number can be found on the product's label following the word 'Batch'.
Search for reports by entering the product batch number.
Batch number can be found on the product's label following the word 'Batch'.
Search for reports by entering the product batch number.
Batch number can be found on the product's label following the word 'Batch'.
Search for reports by entering the product batch number.
Batch number can be found on the product's label following the word 'Batch'.
Search for reports by entering the product batch number.
Batch number can be found on the product's label following the word 'Batch'.
| CAS No. : | 569-58-4 |
| Formula : | C22H23N3O9 |
| M.W : | 473.43 |
| SMILES Code : | O=C(C=C/1)C(C([O-])=O)=CC1=C(C2=CC(C([O-])=O)=C(O)C=C2)\C3=CC(C([O-])=O)=C(O)C=C3.[NH4+].[NH4+].[NH4+] |
| English Name : | Ammonium 5,5'-((3-carboxylato-4-oxocyclohexa-2,5-dien-1-ylidene)methylene)bis(2-hydroxybenzoate) |
| MDL No. : | MFCD00040925 |
* 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.

| Yield | Reaction Conditions | Operation in experiment |
|---|---|---|
| Herstellung von <α-14<i>C</i>>Aluminon; |
| Yield | Reaction Conditions | Operation in experiment |
|---|---|---|
| 86% | With air In water for 12h; Irradiation; |
| Yield | Reaction Conditions | Operation in experiment |
|---|---|---|
| In water |
| Yield | Reaction Conditions | Operation in experiment |
|---|---|---|
| 0.53% | In ethanol; water at 75℃; for 0.3h; | 2.2 Synthesis of alkaline earth metal ion complexes General procedure: A simple strategy was utilized to prepare the targeted alkaline earth metal ion complexes (Scheme 1S). By using, 1:2M ratio from ATA ligand (dark red) and each colorless metal salt that was mixed in EtOH/H2O solvent (3:1). O.947g (2mmol) of ATA ligand was dissolved in 10mL bi-distilled H2O and then mixed with each salt such as, MgCl2 (0.381g), CaCl2 (0.444g), SrCl2 (0.634g) or BaCl2 (0.833g), which dissolved in 30mL EtOH. A colored precipitates were appeared during reflux at 75°C up to 3h, then filtered off and dried in desiccators over CaCl2. The yields of Sr(II) and Ba(II) complexes around 70%, while the yields of Ca(II) and Mg(II) complexes up to 53%. |
| Yield | Reaction Conditions | Operation in experiment |
|---|---|---|
| 0.53% | In ethanol; water at 75℃; for 0.3h; | 2.2 Synthesis of alkaline earth metal ion complexes General procedure: A simple strategy was utilized to prepare the targeted alkaline earth metal ion complexes (Scheme 1S). By using, 1:2M ratio from ATA ligand (dark red) and each colorless metal salt that was mixed in EtOH/H2O solvent (3:1). O.947g (2mmol) of ATA ligand was dissolved in 10mL bi-distilled H2O and then mixed with each salt such as, MgCl2 (0.381g), CaCl2 (0.444g), SrCl2 (0.634g) or BaCl2 (0.833g), which dissolved in 30mL EtOH. A colored precipitates were appeared during reflux at 75°C up to 3h, then filtered off and dried in desiccators over CaCl2. The yields of Sr(II) and Ba(II) complexes around 70%, while the yields of Ca(II) and Mg(II) complexes up to 53%. |
| Yield | Reaction Conditions | Operation in experiment |
|---|---|---|
| 0.7% | In ethanol; water at 75℃; for 0.3h; | 2.2 Synthesis of alkaline earth metal ion complexes General procedure: A simple strategy was utilized to prepare the targeted alkaline earth metal ion complexes (Scheme 1S). By using, 1:2M ratio from ATA ligand (dark red) and each colorless metal salt that was mixed in EtOH/H2O solvent (3:1). O.947g (2mmol) of ATA ligand was dissolved in 10mL bi-distilled H2O and then mixed with each salt such as, MgCl2 (0.381g), CaCl2 (0.444g), SrCl2 (0.634g) or BaCl2 (0.833g), which dissolved in 30mL EtOH. A colored precipitates were appeared during reflux at 75°C up to 3h, then filtered off and dried in desiccators over CaCl2. The yields of Sr(II) and Ba(II) complexes around 70%, while the yields of Ca(II) and Mg(II) complexes up to 53%. |
| Yield | Reaction Conditions | Operation in experiment |
|---|---|---|
| 0.7% | In ethanol; water at 75℃; for 0.3h; | 2.2 Synthesis of alkaline earth metal ion complexes General procedure: A simple strategy was utilized to prepare the targeted alkaline earth metal ion complexes (Scheme 1S). By using, 1:2M ratio from ATA ligand (dark red) and each colorless metal salt that was mixed in EtOH/H2O solvent (3:1). O.947g (2mmol) of ATA ligand was dissolved in 10mL bi-distilled H2O and then mixed with each salt such as, MgCl2 (0.381g), CaCl2 (0.444g), SrCl2 (0.634g) or BaCl2 (0.833g), which dissolved in 30mL EtOH. A colored precipitates were appeared during reflux at 75°C up to 3h, then filtered off and dried in desiccators over CaCl2. The yields of Sr(II) and Ba(II) complexes around 70%, while the yields of Ca(II) and Mg(II) complexes up to 53%. |
| Yield | Reaction Conditions | Operation in experiment |
|---|---|---|
| With ammonia; water; selenium tetrachloride In methanol at 65℃; for 3h; | 2.3. Synthesis of the AAS complexes General procedure: To a solution of AAS (1mmol) dissolved in 25 mL of CH3OH solvent,solution containing 3 mmol of the chloride salt (AuCl3, TaCl5, NbCl5,SeCl4 or TeCl4) dissolved in 25mL of CH3OHwas added, and pHwas optimizedat ~8 using drops of ammoniumsolution (5%). After stirring theresultingmixtures of each chloride at 65 °C for 3 h, colored solid precipitateswere harvested by slow evaporation. The Au(III) ions formed abrownish-red-colored precipitate with AAS, Ta(V) formed red-coloredprecipitate, Nb(V)formed reddish-brown-colored precipitate, Se(IV)formed brown-colored precipitate, where Te (IV) formed orangecoloredprecipitate. These colored precipitates were isolated from thesolutions, thoroughly washed, and dried in an oven at 70°. Complex ofAAS with Au(III) was formulated as [Au3L(H2O)2Cl4], Complexes ofAAS with Se(IV) and Te(IV) ions were formulated as [Se3L(H2O)5Cl7]and [Te3L(H2O)5Cl7], respectively, where the complexes with Nb(V) and Ta(V) ions were formulated as [Nb3L(H2O)2Cl10] and [Ta3L(H2O)2Cl10], respectively (where L5- is the ligand; C22H9O9]. Thesecomplexes were next characterized by elemental, thermal andspectral data. |
| Yield | Reaction Conditions | Operation in experiment |
|---|---|---|
| With ammonia; water; tellurium tetrachloride In methanol at 65℃; for 3h; | 2.3. Synthesis of the AAS complexes General procedure: To a solution of AAS (1mmol) dissolved in 25 mL of CH3OH solvent,solution containing 3 mmol of the chloride salt (AuCl3, TaCl5, NbCl5,SeCl4 or TeCl4) dissolved in 25mL of CH3OHwas added, and pHwas optimizedat ~8 using drops of ammoniumsolution (5%). After stirring theresultingmixtures of each chloride at 65 °C for 3 h, colored solid precipitateswere harvested by slow evaporation. The Au(III) ions formed abrownish-red-colored precipitate with AAS, Ta(V) formed red-coloredprecipitate, Nb(V)formed reddish-brown-colored precipitate, Se(IV)formed brown-colored precipitate, where Te (IV) formed orangecoloredprecipitate. These colored precipitates were isolated from thesolutions, thoroughly washed, and dried in an oven at 70°. Complex ofAAS with Au(III) was formulated as [Au3L(H2O)2Cl4], Complexes ofAAS with Se(IV) and Te(IV) ions were formulated as [Se3L(H2O)5Cl7]and [Te3L(H2O)5Cl7], respectively, where the complexes with Nb(V) and Ta(V) ions were formulated as [Nb3L(H2O)2Cl10] and [Ta3L(H2O)2Cl10], respectively (where L5- is the ligand; C22H9O9]. Thesecomplexes were next characterized by elemental, thermal andspectral data. |
| Yield | Reaction Conditions | Operation in experiment |
|---|---|---|
| With ammonia In methanol at 65℃; for 3h; | 2.3. Synthesis of the AAS complexes General procedure: To a solution of AAS (1mmol) dissolved in 25 mL of CH3OH solvent,solution containing 3 mmol of the chloride salt (AuCl3, TaCl5, NbCl5,SeCl4 or TeCl4) dissolved in 25mL of CH3OHwas added, and pHwas optimizedat ~8 using drops of ammoniumsolution (5%). After stirring theresultingmixtures of each chloride at 65 °C for 3 h, colored solid precipitateswere harvested by slow evaporation. The Au(III) ions formed abrownish-red-colored precipitate with AAS, Ta(V) formed red-coloredprecipitate, Nb(V)formed reddish-brown-colored precipitate, Se(IV)formed brown-colored precipitate, where Te (IV) formed orangecoloredprecipitate. These colored precipitates were isolated from thesolutions, thoroughly washed, and dried in an oven at 70°. Complex ofAAS with Au(III) was formulated as [Au3L(H2O)2Cl4], Complexes ofAAS with Se(IV) and Te(IV) ions were formulated as [Se3L(H2O)5Cl7]and [Te3L(H2O)5Cl7], respectively, where the complexes with Nb(V) and Ta(V) ions were formulated as [Nb3L(H2O)2Cl10] and [Ta3L(H2O)2Cl10], respectively (where L5- is the ligand; C22H9O9]. Thesecomplexes were next characterized by elemental, thermal andspectral data. |
| Yield | Reaction Conditions | Operation in experiment |
|---|---|---|
| With ammonia In methanol at 65℃; for 3h; | 2.3. Synthesis of the AAS complexes General procedure: To a solution of AAS (1mmol) dissolved in 25 mL of CH3OH solvent,solution containing 3 mmol of the chloride salt (AuCl3, TaCl5, NbCl5,SeCl4 or TeCl4) dissolved in 25mL of CH3OHwas added, and pHwas optimizedat ~8 using drops of ammoniumsolution (5%). After stirring theresultingmixtures of each chloride at 65 °C for 3 h, colored solid precipitateswere harvested by slow evaporation. The Au(III) ions formed abrownish-red-colored precipitate with AAS, Ta(V) formed red-coloredprecipitate, Nb(V)formed reddish-brown-colored precipitate, Se(IV)formed brown-colored precipitate, where Te (IV) formed orangecoloredprecipitate. These colored precipitates were isolated from thesolutions, thoroughly washed, and dried in an oven at 70°. Complex ofAAS with Au(III) was formulated as [Au3L(H2O)2Cl4], Complexes ofAAS with Se(IV) and Te(IV) ions were formulated as [Se3L(H2O)5Cl7]and [Te3L(H2O)5Cl7], respectively, where the complexes with Nb(V) and Ta(V) ions were formulated as [Nb3L(H2O)2Cl10] and [Ta3L(H2O)2Cl10], respectively (where L5- is the ligand; C22H9O9]. Thesecomplexes were next characterized by elemental, thermal andspectral data. |
| Yield | Reaction Conditions | Operation in experiment |
|---|---|---|
| With ammonia In methanol at 65℃; for 3h; | 2.3. Synthesis of the AAS complexes General procedure: To a solution of AAS (1mmol) dissolved in 25 mL of CH3OH solvent,solution containing 3 mmol of the chloride salt (AuCl3, TaCl5, NbCl5,SeCl4 or TeCl4) dissolved in 25mL of CH3OHwas added, and pHwas optimizedat ~8 using drops of ammoniumsolution (5%). After stirring theresultingmixtures of each chloride at 65 °C for 3 h, colored solid precipitateswere harvested by slow evaporation. The Au(III) ions formed abrownish-red-colored precipitate with AAS, Ta(V) formed red-coloredprecipitate, Nb(V)formed reddish-brown-colored precipitate, Se(IV)formed brown-colored precipitate, where Te (IV) formed orangecoloredprecipitate. These colored precipitates were isolated from thesolutions, thoroughly washed, and dried in an oven at 70°. Complex ofAAS with Au(III) was formulated as [Au3L(H2O)2Cl4], Complexes ofAAS with Se(IV) and Te(IV) ions were formulated as [Se3L(H2O)5Cl7]and [Te3L(H2O)5Cl7], respectively, where the complexes with Nb(V) and Ta(V) ions were formulated as [Nb3L(H2O)2Cl10] and [Ta3L(H2O)2Cl10], respectively (where L5- is the ligand; C22H9O9]. Thesecomplexes were next characterized by elemental, thermal andspectral data. |