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| Boc-D-Phenylglycine Basic information |
| Boc-D-Phenylglycine Chemical Properties |
| Melting point | 88-91 °C | | alpha | -142 º (c=1% in ethanol) | | Boiling point | 407.2±38.0 °C(Predicted) | | density | 1.182±0.06 g/cm3(Predicted) | | refractive index | -140 ° (C=1, EtOH) | | storage temp. | Keep in dark place,Sealed in dry,Room Temperature | | solubility | DMSO, Methanol | | pka | 3.51±0.10(Predicted) | | form | Crystalline Powder | | color | White | | optical activity | [α]20/D 141.0±5.0°, c = 1% in ethanol | | Water Solubility | Insoluble in water. Slightly soluble in DMSO and methanol. | | BRN | 3033982 | | CAS DataBase Reference | 33125-05-2(CAS DataBase Reference) |
| Safety Statements | 24/25 | | WGK Germany | 3 | | HazardClass | IRRITANT | | HS Code | 29242990 |
| Boc-D-Phenylglycine Usage And Synthesis |
| Chemical Properties | White powder | | Uses | It is a reagent of choice for assignment of absolute configuration of chiral primary amines by 1H NMR, giving better results than Mosher's acid ((R)-(+)-?-Methoxy-?-(trifluoromethyl)-phenyl-acetic acid. αR)-α-[[(1,1-Dimethylethoxy)carbonyl]amino]-benzeneacetic Acid is D-(+)-2-Phenylglycine with Boc protecting group. (αR)-α-[[(1,1-Dimethylethoxy)carbonyl]amino]-benzeneacetic Acid is used as part of a catalyst combination to catalyze regioselective [4 + 2] cycloadditions of β-substituted cyclic enones and polyconjugated malononitriles. It can also be used to catalyze stereoselective preparation of polyfunctional nitrocyclohexene carboxaldehydes. |
| Boc-D-Phenylglycine Preparation Products And Raw materials |
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