Identification | Back Directory | [Name]
Z-VAL-OSU | [CAS]
3496-11-5 | [Synonyms]
Z-VAL-OSU 3496/11/5 CBZ-Val-Osu Z-L-Val-OSu Z-VALINE-OSU Z-L-Val-ONSu CBZ-L-VALINE-OSU Z-L-VALINE HYDROXYSUCCINIMIDESTER N-Cbz-L-valine Succinimidyl Ester Z-VALINE 1-HYDROXYSUCCINIMDE ESTER Z-L-VALINE HYDROXYSUCCINIMIDE ESTER Z-L-VALINE N-HYDROXYSUCCINIMIDE ESTER CBZ-L-VALINE HYDROXYSUCCINIMIDE ESTER CBZ-L-VALINE N-HYDROXYSUCCINIMIDE ESTER N-Carbobenzoxy-L-valine Succinimidyl Ester N-Cbz-L-valine Succinimidyl Ester
Z-Val-OSu N-ALPHA-CBZ-L-VALINE N-HYDROXYSUCCINIMIDE ESTER Z-L-valineN-hydroxysuccinimide ester≥ 98% (HPLC) N-Benzyloxycarbonyl-L-valine N-succinimidyl ester N-(Benzyloxycarbonyl)-L-valine succinimidyl ester N-CARBOBENZOXY-L-VALINE-N-HYDROXYSUCCINIMIDE ESTER N-Benzoxycarbonyl-L-valine N-succiniMidyl ester, 98% BENZYLOXYCARBONYL-L-VALINE N-HYDROXYSUCCINIMIDE ESTER N-alpha-Benzyloxycarbonyl-L-valine succinimidyl ester 2-(benzyloxycarbonylamino)-3-methyl-butyric acid succinimido ester L-Valine,N-[(phenylmethoxy)carbonyl]-, 2,5-dioxo-1-pyrrolidinyl ester (2,5-dioxopyrrolidin-1-yl) 3-methyl-2-(phenylmethoxycarbonylamino)butanoate (S)-2,5-Dioxopyrrolidin-1-yl 2-(((benzyloxy)carbonyl)aMino)-3-Methylbutanoate benzyl (S)-[1-[[(2,5-dioxo-1-pyrrolidinyl)oxy]carbonyl]-2-methylpropyl]carbamate [(S)-1-[[(2,5-Dioxo-1-pyrrolidinyl)oxy]carbonyl]-2-methylpropyl]carbamic acid benzyl ester | [EINECS(EC#)]
222-493-3 | [Molecular Formula]
C17H20N2O6 | [MDL Number]
MFCD00053547 | [MOL File]
3496-11-5.mol | [Molecular Weight]
348.35 |
Chemical Properties | Back Directory | [Melting point ]
114-118℃ | [density ]
1.30±0.1 g/cm3(Predicted) | [storage temp. ]
-15°C | [solubility ]
Soluble in 1mmol in 2mL DCM. | [form ]
Powder | [pka]
10.51±0.46(Predicted) | [color ]
White to off-white | [Optical Rotation]
-21.534°(C=0.01 g/ml Dioxane) | [CAS DataBase Reference]
3496-11-5 |
Hazard Information | Back Directory | [Chemical Properties]
White to offwhite powder | [Uses]
N-Benzyloxycarbonyl-L-valine N-succinimidyl ester, is an amino acid which is widely used in pharmaceutical and food industry. | [Synthesis]
Step 1. To a stirred solution of N-hydroxybutanediimide (1 g, 4 mmol) and CBZ-L-valine (459 mg, 4 mmol) in tetrahydrofuran (THF, 20 mL) was added N,N'-dicyclohexylcarbodiimide (DCC, 908 mg, 4.4 mmol) at 0° C. The reaction was carried out at room temperature. The reaction mixture was stirred at room temperature for 16 hours. After completion of the reaction, the mixture was filtered and the filtrate was concentrated to afford (S)-2,5-dioxopyrrolidin-1-yl 2-(((benzyloxy)carbonyl)amino)-3-methylbutanoate (yield: 90%). | [References]
[1] Chemical Communications, 2015, vol. 51, # 67, p. 13213 - 13216 [2] Organic and Biomolecular Chemistry, 2015, vol. 13, # 28, p. 7736 - 7749 [3] Patent: WO2015/95227, 2015, A2. Location in patent: Page/Page column 133 [4] Journal of Medicinal Chemistry, 2018, vol. 61, # 3, p. 989 - 1000 [5] Journal of the American Chemical Society, 2003, vol. 125, # 22, p. 6677 - 6686 |
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