CAS 30925-18-9
:N-(tert-Butoxycarbonyl)aspartic acid benzyl ester
Description:
N-(tert-Butoxycarbonyl)aspartic acid benzyl ester, with the CAS number 30925-18-9, is a chemical compound commonly used in organic synthesis, particularly in the field of peptide chemistry. This compound features a tert-butoxycarbonyl (Boc) protecting group, which is often employed to protect amine functionalities during chemical reactions. The presence of the benzyl ester moiety enhances the compound's lipophilicity, making it more soluble in organic solvents, which is advantageous for various synthetic applications. The aspartic acid backbone contributes to its potential as a building block in peptide synthesis, allowing for the introduction of specific amino acid sequences. The compound is typically characterized by its stability under acidic and neutral conditions, while it can be deprotected under basic conditions or through specific catalytic methods. Its utility in synthesizing peptides and other complex molecules makes it a valuable intermediate in pharmaceutical and biochemical research. As with all chemical substances, proper handling and safety protocols should be observed due to potential hazards associated with its use.
Formula:C16H21NO6
InChI:InChI=1S/C16H21NO6/c1-16(2,3)23-15(21)17-12(9-13(18)19)14(20)22-10-11-7-5-4-6-8-11/h4-8,12H,9-10H2,1-3H3,(H,17,21)(H,18,19)/t12-/m0/s1
InChI key:InChIKey=LDRWTKQWSXGSTM-LBPRGKRZSA-N
SMILES:[C@H](C(OCC1=CC=CC=C1)=O)(NC(OC(C)(C)C)=O)CC(O)=O
Synonyms:- (2R)-4-(benzyloxy)-2-[(tert-butoxycarbonyl)amino]-4-oxobutanoic acid (non-preferred name)
- (3S)-3-[(2-Methylpropan-2-yl)oxycarbonylamino]-4-oxo-4-phenylmethoxybutanoic acid
- (3S)-4-(benzyloxy)-3-[(tert-butoxycarbonyl)amino]-4-oxobutanoic acid (non-preferred name)
- (S)-2-(tert-Butoxycarbonylamino)succinic acid benzyl ester
- (S)-4-(Benzyloxy)-3-[(tertbutoxycarbonyl)amino]-4-oxobutanoic acid
- 4-(Benzyloxy)-3-[(Tert-Butoxycarbonyl)Amino]-4-Oxobutanoic Acid (Non-Preferred Name)
- <span class="text-smallcaps">L</span>-Aspartic acid, N-[(1,1-dimethylethoxy)carbonyl]-, 1-(phenylmethyl) ester
- Boc-L-aspartic acid 1-benzyl ester
- Boc-L-aspartic acid a-benzyl ester
- N-(tert-Butoxycarbonyl)-L-aspartic acid α-benzyl ester
- N-(tert-Butoxycarbonyl)aspartic acid 1-benzyl ester
- N-(tert-Butoxycarbonyl)aspartic acid benzyl ester
- N-a-BOC-L-Asp-OBzl
- N-tert-Butoxycarbonyl-<span class="text-smallcaps">L</span>-aspartic acid α-benzyl ester
- α-Benzyl N-(tert-butoxycarbonyl)-<span class="text-smallcaps">L</span>-aspartate
- Boc-Asp-OBzl
- α-Benzyl N-(tert-butoxycarbonyl)-L-aspartate
- See more synonyms
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Found 6 products.
1-Benzyl N-(tert-Butoxycarbonyl)-L-aspartate
CAS:Formula:C16H21NO6Purity:>98.0%(T)(HPLC)Color and Shape:White to Almost white powder to crystalMolecular weight:323.35L-Aspartic acid, N-[(1,1-dimethylethoxy)carbonyl]-, 1-(phenylmethyl) ester
CAS:Formula:C16H21NO6Purity:98%Color and Shape:SolidMolecular weight:323.3410Boc-L-Aspartic acid 1-benzyl ester
CAS:<p>Boc-L-Aspartic acid 1-benzyl ester</p>Formula:C16H21NO6Purity:98%Color and Shape: white solidMolecular weight:323.34g/molBoc-Asp-OBzl
CAS:<p>M03269 - Boc-Asp-OBzl</p>Formula:C16H21NO6Purity:98%Color and Shape:SolidMolecular weight:323.345Boc-Asp-OBzl
CAS:<p>Boc-Asp-OBzl is a hydrolysate that contains aspartic acid and has been shown to inhibit the activity of the enzyme peptidylglycine alpha-amidating monooxygenase. It is an orthogonal inhibitor that can be used to study the role of aspartic acid in peptide synthesis. Boc-Asp-OBzl has also been shown to inhibit rat liver microsomes, with an IC50 value of about 0.4 mM, and it did not affect the activity of vitamin K1 or other enzymes. This inhibitor can also be used in experiments on rat liver microsomes and solubilized rat liver preparations.br></p>Formula:C16H21NO6Purity:Min. 95%Color and Shape:White PowderMolecular weight:323.34 g/mol





