CAS 69610-41-9

1,1-Dimethylethyl (2S)-2-formyl-1-pyrrolidinecarboxylate

Description:

1,1-Dimethylethyl (2S)-2-formyl-1-pyrrolidinecarboxylate, with the CAS number 69610-41-9, is an organic compound characterized by its pyrrolidine ring structure, which is a five-membered nitrogen-containing heterocycle. This compound features a formyl group (-CHO) and a carboxylate group (-COO-) attached to the pyrrolidine ring, contributing to its reactivity and potential applications in organic synthesis. The presence of the tert-butyl group (1,1-dimethylethyl) enhances its steric bulk, which can influence its chemical behavior and interactions. Typically, compounds like this may exhibit properties such as solubility in organic solvents, moderate stability under standard conditions, and potential reactivity in various chemical reactions, including nucleophilic additions or condensation reactions. Its specific applications may vary, but it could be relevant in fields such as medicinal chemistry or materials science, where pyrrolidine derivatives are often explored for their biological activity or as intermediates in synthetic pathways.

Formula: C₁₀H₁₇NO₃

InChI: InChI=1/C10H17NO3/c1-10(2,3)14-9(13)11-6-4-5-8(11)7-12/h7-8H,4-6H2,1-3H3/t8-/m1/s1

InChI key: InChIKey=YDBPZCVWPFMBDH-QMMMGPOBSA-N

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

Synonyms:

• (S)-1-Boc-2-formylpyrrolidine
• (S)-1-tert-Butoxycarbonylpyrrolidine-2-carboxaldehyde
• (S)-2-Formylpyrrolidine-1-carboxylic acid tert-butyl ester
• (S)-N-BOC-Prolinal
• (S)-tert-butyl 2-formylpyrrolidine-1-carboxylate
• 1,1-Dimethylethyl (2S)-2-formyl-1-pyrrolidinecarboxylate
• 1-Pyrrolidinecarboxylic acid 2-formyl-, 1,1-dimethylethyl ester (2S)-
• 1-Pyrrolidinecarboxylic acid, 2-formyl-, 1,1-dimethylethyl ester, (S)-
• Boc-<span class="text-smallcaps">L</span>-prolinal
• Boc-prolinal
• N-(tert-Butoxycarbonyl)-<span class="text-smallcaps">L</span>-prolinal
• N-(tert-Butoxycarbonyl)prolinal
• N-(tert-Butyloxycarbonyl)-(S)-prolinal
• N-Boc-<span class="text-smallcaps">L</span>-prolinal
• N-Boc-L-prolinal
• N-tert-Butoxycarbonyl-(S)-prolinal
• tert-Butoxycarbonyl-<span class="text-smallcaps">L</span>-prolinal
• tert-Butyl (2S)-2-formyl-1-pyrrolidinecarboxylate
• tert-Butyl (S)-2-formylpyrrolidine-1-carboxylate
• tert-butyl (2R)-2-formylpyrrolidine-1-carboxylate
• tert-butyl (2S)-2-formylpyrrolidine-1-carboxylate
• tert-Butoxycarbonyl-L-prolinal
• (S)-BOC-PYRROLIDINE-2-CARBOXALDEHYDE
• (S)-N-Boc-pyrrolidine-2-carboxaldehyde, N-(tert-Butoxycarbonyl)-L-prolinal
• (S)-2-FORMYL-PYRROLIDINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER
• (S)-N-BOC-PYRROLIDINE-2-CARBOXALDEHYDE
• N-T-BOC-L-PROLINAL
• N-(TERT-BUTOXYCARBONYL)-L-PROLINAL
• (S)-(-)-1-BOC-2-PYRROLIDINECARBALDEHYDE
• 2-Formylpyrrolidine-1-carboxylic acid tert-butyl ester

N-Boc-L-prolinal, 96%

CAS: 69610-41-9

Building block for novel nicotinic acetylcholine receptor ligands with cognition-enhancing properties. Used in the synthesis of chiral -amino sulfides and -amino thiols. Used to synthesize anticoagulants. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product po

Formula: C₁₀H₁₇NO₃

Purity: 96%

Color and Shape: Liquid or viscous liquid, Clear colorless to pale yellow to orange

Molecular weight: 199.25

Ref: 02-H26495

Boc-L-prolinal

CAS: 69610-41-9

Formula: C₁₀H₁₇NO₃

Purity: 97%

Color and Shape: Liquid

Molecular weight: 199.2469

Ref: IN-DA0032GG

Boc-L-prolinal

CAS: 69610-41-9

Formula: C₁₀H₁₇NO₃

Molecular weight: 199.25

Ref: 7W-GM3676

N-t-BOC-L-Prolinal

CAS: 69610-41-9

N-t-BOC-L-Prolinal

Formula: C₁₀H₁₇NO₃

Purity: 98+%

Color and Shape: light brown liquid

Molecular weight: 199.25g/mol

Ref: 54-OR316013

Boc-L-prolinal

CAS: 69610-41-9

Boc-L-prolinal is a stereoselective enolate that has been used in the synthesis of organometallic compounds. It is also used in the preparation of monoclonal antibodies, which are proteins that are produced by the immune system to help fight off infections. Boc-L-prolinal has been shown to be an effective agent for treating many cancers, including breast cancer and melanoma. In addition, it has been shown to inhibit epidermal growth factor (EGF) and other growth factors, which may be due to its ability to induce apoptotic signaling. Boc-L-prolinal also contains a carbonyl group, which can undergo acidolysis reactions with nucleophiles such as water or alcohols.

Formula: C₁₀H₁₇NO₃

Purity: Min. 95%

Color and Shape: Colorless Clear Liquid

Molecular weight: 199.25 g/mol

Ref: 3D-FB50564

N-BOC-L-Prolinal

CAS: 69610-41-9

Formula: C₁₀H₁₇NO₃

Purity: 97%

Color and Shape: Liquid

Molecular weight: 199.25

Ref: 10-F043496