Acidum methylboronic CAS 13061-96-6 Puritas > 98.0% Factory High Quality
Manufacturer Supple Quality, Commercial Productio
Nomen chemicum: Acidum methylboronicum CAS: 13061-96-6
| Nomen chemicum | Acidum methylboronicum |
| Synonyma | Methaneboronic Acidum |
| CAS Number | 13061-96-6 |
| CATTUS Number | RF-PI1437 |
| Stock Status | In Stock, Productio Ascendite ad Tons |
| Formulae hypotheticae | CH5BO2 |
| M. Pondus | 59.86 |
| Brand | Ruifu Chemical |
| Item | Specifications |
| Aspectus | Crystalli albi |
| Puritas / Analysis Methodus | >98.0% |
| Liquescens punctum | 87.0~94.0℃ |
| 1H NMR | Congruunt cum Structure |
| Infrared Imaginis | Conformat ut Structure |
| Totalis immunditias | <2.00% |
| Test Standard | Enterprise Standard |
| Consuetudinem | Pharmaceutical intermedia |
sarcina: Utrem, aluminium foil, sacculum, 25kg/cardboard Drum, vel secundum exigentiam emptoris.
Repono Condition:Repone in vasis signatis in loco frigido et sicco;A luce et humore protege.
Acidum methylboricum (CAS: 13061-96-6) est derivatio methylata acidi boronici, clausus aedificii versus varia media in coniunctione suzuki, multas applicationes in synthesi organica habet.Acidum methylboronicum pro reagens adhiberi potest: In palladio catalyzed Stille et Suzuki-Miyaura commissuras crucis.Proin in-calefactum palladium heterogeneum (Pd) -catalytized reactiones.In ruthenium (Ru) catalystae motus silylationes Parare bis (aminotropone) titanium (Ti) catalystae ad polymerizationes ethylenes.In bromoaminocyclizatione et bromoaminocyclizatione enantioselectivae asymmetricae utentes catalystae amino-thiocarbamate.Praeparare aedificium commune ad caudices veneficiis et agrochemicis.Para chrysin analoga per Suzuki-Miyaura motus copulationis.Parare casein kinase i inhibitores.In functionibus CH divergentibus a pharmacophoria sulfonamide diriguntur in inventione medicamento.In synthesi unsymmetrica monosulfides ex disulfedis per copulationem aeris catalysi cum acidis boronicis.In Palladio catalyzed coitu cum tosylate enol.Intermedium magni momenti est ad praeparationem multorum derivatorum acidorum boriciorum ut (S) vel (R) -2-Methyl-CBS-oxazaborolidines.
