CAS 53100-44-0

1-(1,1-Dimethylethyl) (2S)-5-oxo-1,2-pyrrolidinedicarboxylate

Description:

1-(1,1-Dimethylethyl) (2S)-5-oxo-1,2-pyrrolidinedicarboxylate, with the CAS number 53100-44-0, is a chemical compound characterized by its pyrrolidine ring structure, which is a five-membered cyclic amine. This compound features two carboxylate groups, contributing to its potential as a dicarboxylic acid derivative. The presence of the tert-butyl group (1,1-dimethylethyl) enhances its steric bulk, which can influence its reactivity and solubility in various solvents. The (2S) configuration indicates that it has a specific stereochemistry, which can affect its biological activity and interactions with other molecules. Typically, compounds like this may be of interest in organic synthesis, pharmaceuticals, or agrochemicals due to their unique structural features. Additionally, the oxo group (carbonyl) plays a crucial role in reactivity, potentially participating in various chemical reactions such as nucleophilic attacks or condensation reactions. Overall, this compound exemplifies the complexity and diversity of organic molecules in chemical research and applications.

Formula: C₁₀H₁₅NO₅

InChI: InChI=1S/C10H15NO5/c1-10(2,3)16-9(15)11-6(8(13)14)4-5-7(11)12/h6H,4-5H2,1-3H3,(H,13,14)/t6-/m0/s1

InChI key: InChIKey=MJLQPFJGZTYCMH-LURJTMIESA-N

SMILES: C(OC(C)(C)C)(=O)N1[C@H](C(O)=O)CCC1=O

Synonyms:

• (2S)-1-[(2-Methylpropan-2-yl)oxycarbonyl]-5-oxopyrrolidine-2-carboxylic acid
• (2S)-1-[(tert-Butoxy)carbonyl]-5-oxopyrrolidine-2-carboxylic acid
• (S)-1-(tert-Butoxycarbonyl)-5-oxopyrrolidine-2-carboxylic acid
• (S)-5-Oxo-1,2-pyrrolidinedicarboxylic acid, 1-(1,1-dimethylethyl) ester
• 1,2-Pyrrolidinedicarboxylic acid, 5-oxo-, 1-(1,1-dimethylethyl) ester, (2S)-
• 1,2-Pyrrolidinedicarboxylic acid, 5-oxo-, 1-(1,1-dimethylethyl) ester, (S)-
• 1-(1,1-Dimethylethyl) (2S)-5-oxo-1,2-pyrrolidinedicarboxylate
• 1-(tert-butoxycarbonyl)-5-oxo-L-proline
• BOC-L-Pyroglutamic acid
• Boc-Pyr-Oh
• N-Boc-5-oxo-L-proline
• N-Boc-<span class="text-smallcaps">L</span>-pyroglutamic acid
• N-tert-Butoxycarbonyl-<span class="text-smallcaps">L</span>-pyroglutamic acid
• Z-Leu DCHA
• N-Boc-L-pyroglutamic acid
• 1-(tert-Butyl) hydrogen (S)-5-oxopyrrolidine-1,2-dicarboxylate

N-(tert-Butoxycarbonyl)-L-pyroglutamic Acid

CAS: 53100-44-0

Formula: C₁₀H₁₅NO₅

Purity: >98.0%(T)(HPLC)

Color and Shape: White to Almost white powder to crystal

Molecular weight: 229.23

Ref: 3B-B4083

Boc-Pyr-OH

CAS: 53100-44-0

Bachem ID: 4026369.

Formula: C₁₀H₁₅NO₅

Purity: 99.39%

Color and Shape: White Powder

Molecular weight: 229.23

Ref: 01-4026369

Boc-Pyr-OH

CAS: 53100-44-0

Formula: C₁₀H₁₅NO₅

Purity: 95%

Color and Shape: Solid

Molecular weight: 229.2298

Ref: IN-DA003CN9

(S)-Boc-5-Oxopyrrolidine-2-carboxylic acid

CAS: 53100-44-0

(S)-Boc-5-Oxopyrrolidine-2-carboxylic acid

Formula: C₁₀H₁₅NO₅

Purity: 98%

Color and Shape: white to off-white solid

Molecular weight: 229.2298g/mol

Ref: 54-OR309165

(S)-Boc-5-oxopyrrolidine-2-carboxylic acid

CAS: 53100-44-0

Formula: C₁₀H₁₅NO₅

Purity: ≥ 98.0%

Color and Shape: White to off-white solid

Molecular weight: 229.23

Ref: 7W-GM0030

Boc-Pyr-OH

CAS: 53100-44-0

Boc-Pyr-OH is a synthetic compound with medical applications. It is used as an anti-inflammatory agent and has been shown to be effective in the treatment of mouse tumor cells. Boc-Pyr-OH binds to plasma proteins and can be detected in the blood following administration. The drug has a high affinity for chloride ions, which may be due to its trifluoroacetyl group. The drug has two homologues: Boc-Pyr-Cl and Boc-Pyr-Br.

Formula: C₁₀H₁₅NO₅

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 229.23 g/mol

Ref: 3D-FB33212

(S)-Boc-5-Oxopyrrolidine-2-carboxylic acid

CAS: 53100-44-0

Purity: 97%

Molecular weight: 229.23

Ref: 10-F955048

Boc-Pyr-OH

Controlled Product

CAS: 53100-44-0

Formula: C₁₀H₁₅NO₅

Color and Shape: Neat

Molecular weight: 229.23

Ref: TR-B665195