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CAS No.: | 2304-94-1 |
---|---|
Name: | Carbobenzyloxy-beta-alanine |
Article Data: | 43 |
Molecular Structure: | |
Formula: | C11H13NO4 |
Molecular Weight: | 223.229 |
Synonyms: | b-Alanine, N-carboxy-, N-benzylester (6CI,7CI,8CI);3-(Benzyloxycarbonylamino)propanoic acid;3-[N-(Benzyloxycarbonyl)amino]propionic acid;Carbobenzoxy-b-alanine;N-(Benzyloxycarbonyl)-b-alanine;N-CBZ-b-alanine;N-Carbobenzoxy-b-alanine;N-Carbobenzyloxy-b-alanine;N-[(Phenylmethoxy)carbonyl]-b-alanine;NSC 17161;NSC 28943;NSC 657842;Z-β-Ala-OH;Z-b-Ala-OH; |
EINECS: | 218-967-4 |
Density: | 1.249 g/cm3 |
Melting Point: | 100-105 °C |
Boiling Point: | 435.9 °C at 760 mmHg |
Flash Point: | 217.4 °C |
Appearance: | White powder |
Hazard Symbols: | Xn |
Risk Codes: | 22-41 |
Safety: | 26-39 |
PSA: | 75.63000 |
LogP: | 1.77840 |
benzyl chloroformate
3-amino propanoic acid
3-(benzyloxycarbonylamino)propanoic acid
Conditions | Yield |
---|---|
With sodium hydroxide In water at 0 - 20℃; | 99% |
With sodium carbonate In 1,4-dioxane; water at 20℃; | 96% |
With sodium carbonate In 1,4-dioxane; water at 0 - 20℃; | 92% |
3-[(N-benzyloxycarbonyl)amino]propanol
3-(benzyloxycarbonylamino)propanoic acid
Conditions | Yield |
---|---|
With NADH oxidase; horse liver alcohol dehydrogenase Enzymatic reaction; | 10% |
Conditions | Yield |
---|---|
With L-Phenylalanine amide; sodium chloride; calcium chloride In N,N-dimethyl-formamide at 25℃; for 3h; pH=8; aq. buffer; | A 7.4% B n/a |
3-(benzyloxycarbonylamino)-propionic acid methyl ester
3-(benzyloxycarbonylamino)propanoic acid
Conditions | Yield |
---|---|
With sodium hydroxide |
succinic acid anhydride
benzyl alcohol
3-(benzyloxycarbonylamino)propanoic acid
Conditions | Yield |
---|---|
(i) tBu3SnN3, dioxane, (ii) /BRN= 878307/, (iii) aq. NaOH; Multistep reaction; | |
(i) nBu3SnN3, THF, (ii) /BRN= 878307/; Multistep reaction; |
N-carbobenzoxy-β-alanine-p-nitrophenyl ester
A
4-nitro-phenol
B
3-(benzyloxycarbonylamino)propanoic acid
Conditions | Yield |
---|---|
With 1H-imidazole; water In ethanol at 25℃; Mechanism; Kinetics; phosphate buffer (pH=8.05); |
N-benzyloxycarbonyl-L-aspartic acid anhydride
A
3-(benzyloxycarbonylamino)propanoic acid
B
N-Cbz-Ala
Conditions | Yield |
---|---|
With hydrogenchloride; bis(1,5-cyclooctadiene)nickel (0); N,N,N,N,-tetramethylethylenediamine In tetrahydrofuran for 8h; Product distribution; Heating; Further complex ligands.; | |
With hydrogenchloride; [2,2]bipyridinyl; bis(1,5-cyclooctadiene)nickel (0) 1.) THF, reflux, 8h.; Yield given. Multistep reaction. Yields of byproduct given; | |
With hydrogenchloride; bis(1,5-cyclooctadiene)nickel (0); N,N,N,N,-tetramethylethylenediamine 1.) THF, reflux, 8h.; Yield given. Multistep reaction. Yields of byproduct given; |
3-(((benzyloxy)carbonyl)amino)propionic tert-butyl ester
3-(benzyloxycarbonylamino)propanoic acid
Conditions | Yield |
---|---|
With trifluoroacetic acid for 0.5h; |
1-diazo-3-(N-benzyloxycarbonyl)amino-2-propanone
3-(benzyloxycarbonylamino)propanoic acid
Conditions | Yield |
---|---|
silver trifluoroacetate In 1,4-dioxane; water for 0.5h; Wolff rearrangement; sonication; | |
With silver benzoate In 1,4-dioxane; water at 110℃; under 3102.97 Torr; for 0.0166667h; Wolff rearrangement; Microwave irradiation; Closed vessel; |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1.1: ClCOOEt; N-methylmorpholine / tetrahydrofuran / 0.25 h / -15 °C 1.2: tetrahydrofuran; CH2Cl2 / -15 - 20 °C 2.1: CF3COOAg / dioxane; H2O / 0.5 h / sonication View Scheme |
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