Cbz-N-methyl-L-valine
Cbz-N-methyl-L-valine Basic information
- Product Name:
- Cbz-N-methyl-L-valine
- Synonyms:
-
- BENZYLOXYCARBONYL-N-ALPHA-METHYL-L-VALINE
- BENZYLOXYCARBONYL-N-METHYL-L-VALINE
- N-Cbz-N-methyl-L-valine
- 3-methyl-2-[methyl(phenylmethoxycarbonyl)amino]butanoic acid
- (S)-2-((benzyloxycarbonyl)(methyl)amino)-3-methylbutanoic acid
- (2S)-2-[[(benzyloxy)carbonyl](Methyl)aMino]-3-Methylbutanoic acid
- (S)-N-(Benzyloxycarbonyl)-N-Methylvaline
- CBZ-N-.ALPHA.-METHYL-L-VALINE
- CAS:
- 42417-65-2
- MF:
- C14H19NO4
- MW:
- 265.3
- Product Categories:
-
- Amino Acid Derivatives
- Mol File:
- 42417-65-2.mol
Cbz-N-methyl-L-valine Chemical Properties
- Melting point:
- 68-70 °C(lit.)
- Boiling point:
- 407.1±34.0 °C(Predicted)
- Density
- 1.166±0.06 g/cm3(Predicted)
- storage temp.
- Sealed in dry,Room Temperature
- solubility
- Chloroform (Slightly), DMSO (Slightly), Ethanol (Slightly), Methanol (Slightly)
- pka
- 4.01±0.10(Predicted)
- form
- Crystalline Solid
- color
- White
- Major Application
- peptide synthesis
- InChI
- 1S/C14H19NO4/c1-10(2)12(13(16)17)15(3)14(18)19-9-11-7-5-4-6-8-11/h4-8,10,12H,9H2,1-3H3,(H,16,17)/t12-/m0/s1
- InChIKey
- NNEHOKZDWLJKHP-LBPRGKRZSA-N
- SMILES
- CC(C)[C@H](N(C)C(=O)OCc1ccccc1)C(O)=O
- CAS DataBase Reference
- 42417-65-2(CAS DataBase Reference)
Safety Information
- Safety Statements
- 36/37
- WGK Germany
- 3
- Storage Class
- 11 - Combustible Solids
MSDS
- Language:English Provider:SigmaAldrich
Cbz-N-methyl-L-valine Usage And Synthesis
Chemical Properties
White powder
Uses
(S)-N-(Benzyloxycarbonyl)-N-methylvaline has been used as a reactant in the synthesis of a biologically active cyclodepsipeptide destruxin E which is a potent negative regulator of osteoclast morphology.
reaction suitability
reaction type: solution phase peptide synthesis
Synthesis
Under argon atmosphere, 60% sodium hydroxide (5 g, 0.125 mol) was added in one portion to a stirred mixture of Cbz-L-valine (9.5 g, 0.038) in anhydrous THF (150 mL) at 0??C and stirred simultaneously for 30 minutes. mol) in anhydrous THF (150 mL) and stir for 30 minutes. Iodomethane (20 mL, 0.32 mol) was added and the resulting mixture was stirred overnight at room temperature. Ice water (200mL) was poured into the mixture at 0??C and the resulting mixture was extracted with ether (2x200mL). The aqueous layer was acidified to pH using dilute HCl solution 1.5 and extracted with ethyl acetate (3x200mL). The combined organic extracts were washed with saturated sodium thiosulfate solution (100 mL), dried (Na2SO4) and evaporated in vacuo to give N and evaporated in vacuum to give N-Cbz-N-methyl-L-valine (5 g, 55%) as a colorless viscous oil which can be used in the next step without purification.
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