A1359412
Benzophenone imine , 95% , 1013-88-3
| Pack Size | Price | Stock | Quantity |
| 5G | RMB23.20 | In Stock |
|
| 25G | RMB46.40 | In Stock |
|
| 100G | RMB150.40 | In Stock |
|
| 500g | RMB673.60 | In Stock |
|
| others | Enquire |
Update time: 2022-07-08
PRODUCT Properties
| Melting point: | -30 °C |
| Boiling point: | 108 °C/1 mmHg |
| Density | 1.08 |
| vapor pressure | 0.082Pa at 20℃ |
| refractive index | 1.62 |
| Flash point: | 109 °C - closed cup |
| storage temp. | Inert atmosphere,Room Temperature |
| solubility | DMSO (Slightly), Ethyl Acetate (Slightly) |
| pka | pK1:6.82 (25°C) |
| form | clear liquid |
| color | Colorless to Light orange to Yellow |
| Water Solubility | 0.3 g/L (25 ºC) |
| BRN | 1100371 |
| Major Application | diagnostic assay manufacturing hematology histology |
| InChI | 1S/C13H11N/c14-13(11-7-3-1-4-8-11)12-9-5-2-6-10-12/h1-10,14H |
| InChIKey | SXZIXHOMFPUIRK-UHFFFAOYSA-N |
| SMILES | N=C(c1ccccc1)c2ccccc2 |
| CAS DataBase Reference | 1013-88-3(CAS DataBase Reference) |
| NIST Chemistry Reference | Benzenemethanimine, «alpha»-phenyl-(1013-88-3) |
Description and Uses
Useful in the preparation of nitrile ylide dimers.Benzophenone imine as ammonia surrogate. As intermediate material for synthesis of organic chemicals. Catalytic enantioselective alkylation of the benzophenone imine of glycine t-butyl ester using phosphazene (Schwesinger) bases and chiral quaternary ammonium salts yields either enantiomer of amino acid derivatives in excellent yield.
Safety
| Symbol(GHS) |  GHS07 |
| Signal word | Warning |
| Hazard statements | H315-H319-H335 |
| Precautionary statements | P261-P264-P271-P280-P302+P352-P305+P351+P338 |
| target organs | Respiratory system |
| PPE | Eyeshields, Gloves, type ABEK (EN14387) respirator filter |
| Hazard Codes | Xi,N,Xn |
| Risk Statements | 36/37/38-51/53-38-22 |
| Safety Statements | 26-36-61-37 |
| RIDADR | UN3082 |
| WGK Germany | 3 |
| HS Code | 29252900 |
| Storage Class | 10 - Combustible liquids |
| Hazard Classifications | Eye Irrit. 2 Skin Irrit. 2 STOT SE 3 |
| REACH Registrations | Active |
