(S)-Alpha-(fmoc-amino)-cyclobutaneacetic acid

Basic Information

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CAS Number

1391630-31-1

Molecular Formula

C21H21NO4

Molecular Weight

351.4 g/mol

Chemical Classification

Basic Chemical Raw Materials Organic Chemicals Carboxylic Acids

Basic Chemical Raw Materials Organic Chemicals Ethers

Fine Chemicals Dyes and Pigments Organic Dyes

Fine Chemicals Surfactants Anionic Surfactants

Basic Physical Properties

SMILES

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O=C(N[C@@H](C1CCC1)C(=O)O)OCC1c2ccccc2c2c1cccc2

InChI

InChI=1S/C21H21NO4/c23-20(24)19(13-6-5-7-13)22-21(25)26-12-18-16-10-3-1-8-14(16)15-9-2-4-11-17(15)18/h1-4,8-11,13,18-19H,5-7,12H2,(H,22,25)(H,23,24)/t19-/m0/s1

InChIKey

TXLUWFPQLXODBP-IBGZPJMESA-N

LogP

3.778400000000003

Topological Polar Surface Area

75.63000000000001 Å²

Hydrogen Bond Donor/Acceptor

2 / 5

Complexity

510

Synonyms & References

English

(S)-a-(Fmoc-amino)cyclobutaneacetic acid
(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-cyclobutylacetic acid
(2S)-2-cyclobutyl-2-(9H-fluoren-9-ylmethoxycarbonylamino)acetic acid
(S)-Fmoc-Cyclobutylglycine, AldrichCPR
(S)-alpha-(Fmoc-amino)cyclobutaneacetic acid
(S)-Alpha-(fmoc-amino)-cyclobutaneacetic acid
P18455
(2S)-2-CYCLOBUTYL-2-({[(9H-FLUOREN-9-YL)METHOXY]CARBONYLAMINO)ACETIC ACID
(2S)-2-cyclobutyl-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)acetic acid

MDL Number

MFCD09839305

FAQ

What regulatory guidelines apply to (S)-Alpha-(fmoc-amino)-cyclobutaneacetic acid (CAS: 1391630-31-1)?

The (S)-Alpha-(fmoc-amino)-cyclobutaneacetic acid (CAS: 1391630-31-1) is subject to various regulatory guidelines including GHS for hazardous communication, REACH for registration, evaluation, authorization, and restriction of chemicals in the EU, and FDA/EPA requirements for safe handling and disposal in the USA. It is advisable to consult specific guidelines based on the intended use and jurisdiction.

Are there alternatives to (S)-Alpha-(fmoc-amino)-cyclobutaneacetic acid in synthesis?

Yes, there are alternatives to (S)-Alpha-(fmoc-amino)-cyclobutaneacetic acid in synthesis, such as other protected amino acids or fmoc-protected derivatives. Common alternatives include (R)-Alpha-(fmoc-amino)-cyclobutaneacetic acid or unprotected cyclobutaneacetic acid derivatives, which can offer similar functionalities with varying degrees of reactivity.

What is the market or research trend for (S)-Alpha-(fmoc-amino)-cyclobutaneacetic acid?

The market and research trend for (S)-Alpha-(fmoc-amino)-cyclobutaneacetic acid is growing due to its applications in medicinal chemistry and peptide synthesis. Its use in developing new drugs and therapeutic peptides is increasing, driven by the need for specific stereochemistry control and functional groups. Research is also focusing on its role in drug discovery and development.

How should waste containing (S)-Alpha-(fmoc-amino)-cyclobutaneacetic acid be handled?

Waste containing (S)-Alpha-(fmoc-amino)-cyclobutaneacetic acid (CAS: 1391630-31-1) should be collected in appropriate containers and disposed of according to local regulations. Incineration or professional waste disposal services are recommended. Proper handling includes ensuring the waste is neutralized and decontaminated if necessary, and following environmental protection precautions to minimize environmental impact.