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Maximum quantity allowed is 999
| Size | Unit Price | Hyderabad | Japan* | Quantity |
|---|---|---|---|---|
| 1G |
₹3,500.00
|
Contact Us | ≥100 |
|
| 5G |
₹15,900.00
|
Contact Us | ≥100 |
|
| 25G |
₹71,000.00
|
4 | ≥100 |
|
*Upon orders receipt, Hyderabad stocks will be dispatched on the same day.
*Items available in Japan warehouse will be dispatched in 10-12 working days.
*INR price is exclusive of domestic taxes applicable.
*TCI frequently reviews storage conditions to optimize them. Please note that the latest information on the storage temperature for the products is described on our website.
| Product Number | T1350 |
Purity / Analysis Method
|
>97.0%(T) |
| Molecular Formula / Molecular Weight | C__7__2H__6__0P__4Pd = 1,155.59 |
| Physical State (20 deg.C) | Solid |
Storage Temperature
|
Frozen (-20°C) |
| Store Under Inert Gas | Store under inert gas |
| Condition to Avoid | Air Sensitive,Heat Sensitive |
| CAS RN | 14221-01-3 |
| Reaxys Registry Number | 11604118 |
| PubChem Substance ID | 87577117 |
| MDL Number | MFCD00010012 |
| Appearance | Light yellow to Amber to Dark green powder to crystaline |
| Purity(Chelometric Titration) | 97.0 to 106.0 % |
| IR | confirm to structure |
| Melting Point | 115 °C |
| Pictogram |
|
| Signal Word | Warning |
| Hazard Statements | H302 : Harmful if swallowed. H413 : May cause long lasting harmful effects to aquatic life. |
| Precautionary Statements | P501 : Dispose of contents/ container to an approved waste disposal plant. P273 : Avoid release to the environment. P270 : Do not eat, drink or smoke when using this product. P264 : Wash skin thoroughly after handling. P301 + P312 + P330 : IF SWALLOWED: Call a POISON CENTER/doctor if you feel unwell. Rinse mouth. |

(3-Formylphenyl)boronic acid (480 mg, 3.2 mmol) and 4-chloro-3,5-dimethyl-phenol (500 mg, 3.2 mmol) and tetrakis(triphenylphosphine)palladium(0) (55 mg, 0.048 mmol, 1.5 mol%) were dissolved in degassed ethanol (20 mL). A solution of sodium carbonate (250 mg, 2.4 mmol) in water (5 mL) was added to the solution, and the mixture was stirred for 5 h at 75 °C. The reaction mixture was cooled to room temperature and filtered. The filtrate was concentrated, cooled Et2O (15 mL) was added and filtered to remove insoluble. The filtrate was concentrated to give the desired product as a pale yellow crystalline solid (506 mg, 2.24 mmol, 70%).
Ethanol was degassed by purging with N2.
The reaction mixture was monitored by TLC (hexane : ethyl acetate = 2 : 3, Rf = 0.8).
1H NMR (400 MHz, CDCl3); δ 10.09 (s, 1H), 8.13 (s, 1H), 7.90 (t, J = 6.8 Hz, 2H), 7.65 (t, J = 7.6 Hz, 1H), 6.56 (s, 2H), 4.79 (s, 1H), 2.36 (s, 6H).

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