N-Boc-L-alaninol
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- CAS-Nr.
- 79069-13-9
- Englisch Name:
- N-Boc-L-alaninol
- Synonyma:
- tert-butyl (S)-(1-hydroxypropan-2-yl)carbamate;BOC-L-ALANINOL;N-TERT-BUTOXYCARBONYL-L-ALANINOL;BOC-ALANINOL;BOC-L-ALA-OL;(S)-2-(TERT-BUTOXYCARBONYLAMINO)-1-PROPANOL;Ark047;BOC-ALA-OL;Boc-Alaninnol;Boc-L-alanino
- CBNumber:
- CB6361433
- Summenformel:
- C8H17NO3
- Molgewicht:
- 175.23
- MOL-Datei:
- 79069-13-9.mol
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N-Boc-L-alaninol Eigenschaften
- Schmelzpunkt:
- 59-62 °C(lit.)
- alpha
- -11 º (c=1, chloroform)
- Siedepunkt:
- 276.4±23.0 °C(Predicted)
- Dichte
- 1.025±0.06 g/cm3(Predicted)
- Brechungsindex
- -8.6 ° (C=1.2, MeOH)
- storage temp.
- Sealed in dry,2-8°C
- L?slichkeit
- almost transparency in Methanol
- pka
- 12.11±0.46(Predicted)
- Aggregatzustand
- Crystalline Powder or Lumps
- Farbe
- White
- Optische Aktivit?t
- [α]20/D 11°, c = 1 in chloroform
- BRN
- 3648840
- InChI
- InChI=1S/C8H17NO3/c1-6(5-10)9-7(11)12-8(2,3)4/h6,10H,5H2,1-4H3,(H,9,11)/t6-/m0/s1
- InChIKey
- PDAFIZPRSXHMCO-LURJTMIESA-N
- SMILES
- C(OC(C)(C)C)(=O)N[C@@H](C)CO
- CAS Datenbank
- 79069-13-9(CAS DataBase Reference)
N-Boc-L-alaninol 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 to off-white powder
Verwenden
Boc-L-alanine (N-Boc-L-alaninol) is a versatile amino acid derivative widely utilized in peptide synthesis and pharmaceutical research. This compound features a tert-butoxycarbonyl (Boc) protecting group, which enhances its stability and reactivity, making it an essential building block for the synthesis of various peptides and proteins. Its unique structure allows for selective deprotection under mild conditions, facilitating the production of complex molecules in a controlled manner.
N-Boc-L-alaninol Upstream-Materialien And Downstream Produkte
Upstream-Materialien
Downstream Produkte
N-Boc-L-alaninol Anbieter Lieferant Produzent Hersteller Vertrieb H?ndler.
Global( 446)Lieferanten
79069-13-9()Verwandte Suche:
- N-BOC-S-ALANINOL
- N-ALPHA-T-BOC-L-ALANINOL
- N-ALPHA-TERT-BUTYLOXYCARBONYL-L-ALANINOL
- N-T-BUTOXYCARBONYL-L-ALANINOL
- N-T-BOC-L-ALANINOL
- Boc-Ala-ol~(S)-2-(Boc-amino)-1-propanol~N-(tert-Butoxycarbonyl)-L-alaninol
- Butoxycarbonylalaninol
- Carbamic acid, [(1S)-2-hydroxy-1-methylethyl]-, 1,1-dimethylethyl ester (9CI)
- (S)-2-(Boc-amino)-1-propanol=N-(tert-Butoxycarbonyl)-L-alaninol
- N-t-Boc-L-Alaninol=Boc-Ala-ol
- N-Boc-L-alaninol,98%
- N-TERT-BOC-L-ALANINOL
- L-BOC-ALaninoL
- (S)-2-(t-Butoxycarbonylamino)-1-propanol
- N-ALPHA-T-BUTYLOXYCARBONYL-L-ALANINOL, (S)-2-(T-BUTYLOXYCARBONYL-AMINO)-1-PROPANOL
- (2-Hydroxy-1-methyl-ethyl)-carbamic acid tert-butyl ester
- N-Boc-L-alaninol, Boc-L-alaninol, (S)-(-)-2-(tert-Butoxycarbonylamino)-1-propanol
- N-Boc-Alaninol
- (S)-tert-butyl 1-hydroxypropan-2-ylcarbamate
- Ark047
- (2S)-2-Aminopropan-1-ol, N-BOC protected
- tert-Butyl [(2S)-1-hydroxypropan-2-yl]carbamate, L-Alaninol, N-BOC protected
- BOC-ALA-OL
- BOC-(S)-2-AMINO-1-PROPANOL
- (S)-(-)-2-(TERT-BUTOXYCARBONYLAMINO)-1-PROPANOL
- (S)-2-(TERT-BUTYLOXYCARBONYL-AMINO)-1-PROPANOL
- (S)-(-)-2-(BOC-AMINO)-1-PROPANOL
- (S)-2-(BOC-AMINO)-1-PROPANOL
- TERT-BUTYL (1S)-2-HYDROXY-1-METHYLETHYLCARBAMATE
- N-BOC-L-ALANINOL
- N-Boc-L-alaninol
(S)-2-(tert-Butoxycarbonylamino)-1-propanol
- Boc-Alaninnol
- N-boc-l-alanine alcohol
- tert-butyl N-[(2S)-1-hydroxypropan-2-yl]carbamate
- N-(tert-Butoxycarbonyl)-L-alaninol >
- Carbamic acid, N-[(1S)-2-hydroxy-1-methylethyl]-, 1,1-dimethylethyl ester
- N-Boc-L-alaninol(For export only)
- N-Boc-L-alaninol USP/EP/BP
- tert-butyl N-[(1S)-2-hydroxy-1-methyl-ethyl]carbamate
- N-TERT-BUTOXYCARBONYL-L-ALANINOL
- BOC-ALANINOL
- BOC-L-ALANINOL
- BOC-L-ALA-OL
- (S)-2-(TERT-BUTOXYCARBONYLAMINO)-1-PROPANOL
- tert-butyl (S)-(1-hydroxypropan-2-yl)carbamate
- 1,1-Dimethylethyl N-[(1S)-2-hydroxy-1-methylethyl]carbamate
- BOC-L propanol
- (S)-2-t-butoxycarbonylaminopropan-1-ol
- Boc-L-alanino
- N-Boc-L-Alaninol /(S)-2-(Boc-amino)-1-propanol
- Boc-L-propanemol
- 79069-13-9
- C8H16NO3
- CH3CHNHCO2CCH33CH2OH
- ALCOHOL
- Organic Building Blocks
- Peptide Synthesis
- Specialty Synthesis
