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Nalpha-FMOC-L-Asparagine

  • Product Name Nalpha-FMOC-L-Asparagine
  • cas 71989-16-7
  • purity 99%
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Quality products?make an important contribution to long-term revenue and profitability. Good factory exports good Nalpha-FMOC-L-Asparagine 71989-16-7

1.What is the Nalpha-FMOC-L-Asparagine ?

white to light yellow crystal powde

Nalpha-FMOC-L-Asparagine, also known as Nα-Fmoc-L-asparagine, is an N-Fmoc-protected form of L-Asparagine (A790005), an amino acid that plays a crucial role in protein synthesis and has potential applications in cancer therapy. L-Asparagine was first isolated by Robiquet and Vauquelin from asparagus juice, which is a high source of this amino acid. The N-Fmoc protection group is used to prevent unwanted side reactions during the synthesis process.

2.What is the CAS number for Nalpha-FMOC-L-Asparagine ?

The CAS number of Nalpha-FMOC-L-Asparagine is 71989-16-7.

3.What are another words for Nalpha-FMOC-L-Asparagine ?

Synonyms?for?Nalpha-FMOC-L-Asparagine 71989-16-7:N-(9-Fluorenylmethoxycarbonyl)-L-asparagine;Fmoc-L-Asn-OH;N-α-Fmoc-L-asparagine;N2-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-asparagine;Fmoc-L-Asnparagine;(2S)-3-carbamoyl-2-(9H-fluoren-9-ylmethoxycarbonylamino)propanoate;3-carbamoyl-2-(9H-fluoren-9-ylmethoxycarbonylamino)propanoic acid;

4.What is Nalpha-FMOC-L-Asparagine (71989-16-7) used for?

Nα-Fmoc-L-asparagine is an N-Fmoc-protected form of L-Asparagine (A790005). L-Asparagine was first isolated by Robiquet and Vauquelin from asparagus juice (a high source of L-asparagine). L-Asparagine is often incorporated into proteins, and is a basis for some cancer therapies as certain cancerous cells require L-asparagine for growth.

InChI:InChI=1/C19H18N2O5/c20-17(22)9-16(18(23)24)21-19(25)26-10-15-13-7-3-1-5-11(13)12-6-2-4-8-14(12)15/h1-8,15-16H,9-10H2,(H2,20,22)(H,21,25)(H,23,24)/p-1/t16-/m0/s1

Relevant articles related to Nalpha-FMOC-L-Asparagine:

Article

Source

Novel chiral stationary phases based on 3,5-dimethyl phenylcarbamoylated β-cyclodextrin combining cinchona alkaloid moiety

Zhu, Lunan,Zhu, Junchen,Sun, Xiaotong,Wu, Yaling,Wang, Huiying,Cheng, Lingping,Shen, Jiawei,Ke, Yanxiong

, p. 1080 - 1090 (2020/05/25)

New TFA-free cleavage and final deprotection in Fmoc solid-phase peptide synthesis: Dilute HCl in fluoro alcohol

Palladino, Pasquale,Stetsenko, Dmitry A.

supporting information, p. 6346 - 6349 (2013/02/25)

Liquid-chromatography quantitative analysis of 20 amino acids after derivatization with FMOC-CI and its application to different origin Radix isatidis

Zhou, Wei,Zhang, Xiao-Yan,Duan, Geng-Li

experimental part, p. 509 - 515 (2012/01/04)

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