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FMOC-Ala-OH

  • CAS：35661-39-3
  • purity：99%
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What is the FMOC-Ala-OH ?

FMOC-Ala-OH is white to light yellow crystal powder, while it's Molecular Formula is C18H17NO4. N-Fmoc-L-alanine is potentially useful for proteomics studies and solid phase peptide synthesis techniques. Alanine is one of the simplest amino acids - a methyl group as the side chain. This small side chain confers a high degree of flexibility when incorporated into a polypeptide chain. The Fmoc group is typically removed with a base such as pyridine - an orthogonal de-protection strategy to the acid labilie Boc group.

What is the CAS number for FMOC-Ala-OH ?

The CAS number of FMOC-Ala-OH is 35661-39-3.

More information of FMOC-Ala-OH 35661-39-3 are:

Synonyms

(2S)-2-[[[(9H-Fluoren-9-yl)methoxy]carbonyl]amino]propanoicacid;(9-Fluorenylmethoxycarbonyl)-L-alanine;(S)-2-[[[(9H-Fluoren-9-yl)methoxy]carbonyl]amino]propionic acid;(S)-N-Fmoc-alanine;FMOC-Alanine;N-(9-Fluorenylmethoxycarbonyl)alanine;N-9-Fluorenylmethoxycarbonyl-L-alanine;NPC 14688;NSC 334296;Fmoc-Ala-OH;Fmoc-β-Ala-OH;

CAS?Number

35661-39-3

Molecular Formula

C18H17NO4

Molecular Weight

311.337

Density

282 g/cm3

Melting Point

147-153 °C(lit.)

Boiling Point

544.1 °C at 760 mmHg

Flash Point

282.9 °C

HS CODE

29242990

PSA

79.12000

LogP

3.20260

Pka

3.91±0.10(Predicted)

What is FMOC-Ala-OH (35661-39-3) used for?

FMOC-Ala-OH, also known as N-Fmoc-L-alanine, is a synthetic derivative of the naturally occurring amino acid L-alanine. It is characterized by the presence of a 9-fluorenylmethoxycarbonyl (Fmoc) protecting group, which is commonly used in peptide synthesis. FMOC-Ala-OH is a white to light yellow crystalline powder and is known for its high degree of flexibility when incorporated into a polypeptide chain due to the small size of the methyl group as the side chain.

InChI:InChI=1/C18H17NO4/c1-11(17(20)21)19-18(22)23-10-16-14-8-4-2-6-12(14)13-7-3-5-9-15(13)16/h2-9,11,16H,10H2,1H3,(H,19,22)(H,20,21)/p-1/t11-/m0/s1

Articles related to FMOC-Ala-OH:

Article

Source

Fungal Dioxygenase AsqJ Is Promiscuous and Bimodal: Substrate-Directed Formation of Quinolones versus Quinazolinones

Einsiedler, Manuel,Jamieson, Cooper S.,Maskeri, Mark A.,Houk, Kendall N.,Gulder, Tobias A. M.

supporting information, p. 8297 - 8302 (2021/03/01)

Determination of Chemical and Enantiomeric Purity of α-Amino Acids and their Methyl Esters as N-Fluorenylmethoxycarbonyl Derivatives Using Amylose-derived Chiral Stationary Phases

Islam, Md. Fokhrul,Adhikari, Suraj,Paik, Man-Jeong,Lee, Wonjae

, p. 332 - 338 (2019/04/13)

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