BOC-L-Phenylglycinol
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- CAS-Nr.
- 117049-14-6
- Englisch Name:
- BOC-L-Phenylglycinol
- Synonyma:
- BOC-PHG-OL;(S)-N-(TERT-BUTOXYCARBONYL)-2-PHENYLGLYCINOL;tert-butyl (S)-(2-hydroxy-1-phenylethyl)carbamate;Boc-L-Phg-OL;CAS:117049-14-6;Boc-L-phenyglycol;BOC-PHENYLGLYCINOL;BOC-L-PHENYLGLYCINOL;TBOC-L-PHENYLGLYCINOL;Asciminib Impurity 19
- CBNumber:
- CB4287458
- Summenformel:
- C13H19NO3
- Molgewicht:
- 237.3
- MOL-Datei:
- 117049-14-6.mol
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BOC-L-Phenylglycinol Eigenschaften
- Schmelzpunkt:
- 136-139 °C(lit.)
- alpha
- +37°(19℃, c=1, CHCl3)
- Siedepunkt:
- 382.4±35.0 °C(Predicted)
- Dichte
- 1.101±0.06 g/cm3(Predicted)
- storage temp.
- Inert atmosphere,Room Temperature
- pka
- 11.55±0.46(Predicted)
- Aggregatzustand
- powder to crystal
- Farbe
- White to Orange to Green
- Optische Rotation
- [α]19/D +37°, c = 1 in chloroform
- Wasserl?slichkeit
- Insoluble in water.
- BRN
- 4316842
- Major Application
- peptide synthesis
- InChI
- 1S/C13H19NO3/c1-13(2,3)17-12(16)14-11(9-15)10-7-5-4-6-8-10/h4-8,11,15H,9H2,1-3H3,(H,14,16)/t11-/m1/s1
- InChIKey
- IBDIOGYTZBKRGI-LLVKDONJSA-N
- SMILES
- CC(C)(C)OC(=O)N[C@H](CO)c1ccccc1
- CAS Datenbank
- 117049-14-6(CAS DataBase Reference)
BOC-L-Phenylglycinol Chemische Eigenschaften,Einsatz,Produktion Methoden
S-S?tze Betriebsanweisung:
S22:Staub nicht einatmen.
S24/25:Berührung mit den Augen und der Haut vermeiden.
Chemische Eigenschaften
White solid
Verwenden
N-Boc-L-alpha-phenylglycinol is an important raw material and intermediate used in organic Synthesis, pharmaceuticals, agrochemicals and dye fields. Phenylglycinol-derived oxazolopiperidone lactams is used as starting materials for the enantioselective synthesis of piperidine-containing alkaloids.
BOC-L-Phenylglycinol Upstream-Materialien And Downstream Produkte
Upstream-Materialien
Downstream Produkte
BOC-L-Phenylglycinol Anbieter Lieferant Produzent Hersteller Vertrieb H?ndler.
Global( 275)Lieferanten
117049-14-6()Verwandte Suche:
- TBOC-L-PHENYLGLYCINOL
- (S)-N-BOC-2-PHENYLGLYCINOL
- (S)-(+)-N-(TERT-BUTOXYCARBONYL)-2-PHENYLGLYCINOL
- (S)-N-(TERT-BUTOXYCARBONYL)-PHENYLGLYCINOL
- S(+)-2-(BOC)-AMINO-2-PHENYLETHANOL
- ((S)-2-HYDROXY-1-PHENYL-ETHYL)-CARBAMIC ACID TERT-BUTYL ESTER
- (S)-2-(TERT-BUTOXYCARBONYLAMINO)-2-PHENYLETHANOL
- N-T-BOC-L-PHENYLGLYCINOL
- N-T-BUTOXYCARBONYL-L-PHENYLGLYCINOL
- N-ALPHA-T-BOC-L-PHENYLGLYCINOL
- N-BOC-L-ALPHA-PHENYLGLYCINOL
- N-BOC-L-PHENYLGLYCINOL
- N-Boc- L -2-phenylglycinol
- CARBAMIC ACID, [(1S)-2-HYDROXY-1-PHENYLETHYL]-, 1,1-DIMETHYLETHYL ESTER
- BOC-L-PHENYLGLYCINOL
- BOC-PHENYLGLYCINOL
- (S)-(+)-2-(Boc-amino)-2-phenylethanol~Boc-Phg-ol~N-(tert-Butoxycarbonyl)-L-alpha-phenylgycinol
- Boc-L-Alpha-Phenylglycinol
- (S)-(+)-N-(TERT-BUTOXYCARBONYL)-2-PHENYL GLYCINOL, 99% (99% EE/GLC)
- N-BOC-(S)-phenylglycinol
- n-boc-l-à-phenylglycinol
- Boc-L-2-phenylglycinol
- Boc-(S)-2-phenylglycinol
- N-tert-Butoxycarbonyl-L-phenylglycinol
- Boc-L-Phg-OL
- Boc-L-phenylglycinol99.0 +%
- N-Boc-L-ɑ-phenylglycinol, 98%
- NALPHA-tert-Butoxycarbonyl-L-phenylglycinol
- N-(tert-Butoxycarbonyl)-L-2-phenylglycinol
- N-Boc-L-^a-phenylglycinol, 98%
- N-Boc-L-2-phenylglycinol
(S)-2-(tert-Butoxycarbonylamino)-2-phenylethanol
- (S)-N-(t-butoxycarbonyl)-2-phenylglycinol
- (S)-tert-butyl 2-hydroxy-1-phenylethylcarbaMate
- N-boc-L-α-phenylglycinol
- N-Boc-(S)-2-phenylglycinol
- BOC-L-Phenylglycinol USP/EP/BP
- Carbamic acid, N-[(1S)-2-hydroxy-1-phenylethyl]-, 1,1-dimethylethyl ester
- (S)-(+)-2-(Boc-amino)-2-phenyL
- N-(tert-Butoxycarbonyl)-L-2-phenylglycinol >
- Boc-l-phenylglycine glycol
- N-(2-hydroxy-1-phenylethyl)carbamic acid tert-butyl ester
- (S)-N-(TERT-BUTOXYCARBONYL)-2-PHENYLGLYCINOL
- tert-butyl (S)-(2-hydroxy-1-phenylethyl)carbamate
- Boc-L-phenyglycol
- Asciminib Impurity 19
- (+)-N-boc-L-alpha-phenylglycinol
- CAS:117049-14-6
- (+)-N-Boc-L-α-phenylglycinol
- (+)-N-Boc-L-α-phenylglycinol
- BOC-PHG-OL
- 117049-14-6
- Amino Alcohols
- Amino Acid Derivatives
- Specialty Synthesis
- Peptide Synthesis
- Amino Acid Derivatives
- Amino Acids
