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Detail of "30924-93-7"

  • CAS Number:
  • 30924-93-7
  • Name:

  • L-Glutamicacid, N-[(1,1-dimethylethoxy)carbonyl]-, 1-(phenylmethyl) ester

  • Superlist Name:
  • Boc-L-Glutamic acid 1-benzyl ester
  • Molecular Structure:
  • Formula:
  • C17H23NO6
  • Molecular Weight:
  • 337.37
  • Deleted CAS:
  • 60738-12-7
  • Synonyms:
  • N-tert-Butoxycarbonyl-L-glutamic acid α-benzyl ester;N-tert-Butoxycarbonyl-L-glutamic acid benzyl ester;Boc-Glu-Obzl;(S)-5-(benzyloxy)-4-(tert-butoxycarbonylamino)-5-oxopentanoic acid;
  • Density:
  • 1.198 g/cm3
  • Boiling Point:
  • 522.6 °C at 760 mmHg
  • Flash Point:
  • 269.859 °C
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CAS No.30924-93-7 Boc-L-Glutamic acid 1-benzyl esterCompetitive Product

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CAS No.30924-93-7 Boc-L-Glutamic acid 1-benzyl ester

Boc-Glu-Obzl,Cas#30924-93-7

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CAS No.30924-93-7 Boc-L-Glutamic acid 1-benzyl ester

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CAS No.30924-93-7 Boc-L-Glutamic acid 1-benzyl ester

Boc-Glu-OBzl (cryst.)

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CAS No.30924-93-7 Boc-L-Glutamic acid 1-benzyl ester

BOC-GLU-OBZL

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CAS No.30924-93-7 Boc-L-Glutamic acid 1-benzyl ester

Product Name Boc-Glu-OBzl Molecular Formula C17H23NO6 Molecular Weight 337.4 Weight Purity (HPLC) ≥98% CAS NO. 30924-93-7

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BOC-GLU-OBZL

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BOC-GLU-OBZL

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BOC-GLU-OBZL

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Reference

Preparation of decapeptide with human interleukin-1-like activity
Preparation of decapeptide with human interleukin-1-like activity. Hirose, Toshihiro; Yasuda, Shuhei; Furuichi, Kiyoshi (Yamanouchi Pharmaceutical Co., Ltd., Japan). Jpn. Kokai Tokkyo Koho JP 03271300 A2 3 Dec 1991 Heisei, 6 pp.Some commonly used reagents like 30924-93-7 and 54613-99-9 are used in this experiment. (Japan). CODEN: JKXXAF. CLASS: ICM: C07K007-06. ICA: A61K037-02. ICI: C07K099-00. APPLICATION: JP 90-70358 19 Mar 1990. DOCUMENT TYPE: Patent CA Section: 34 (Amino Acids, Peptides, and Proteins) Section cross-reference(s): 1 H-Ala-Leu-Gly-Leu-Lys-Glu-Lys-Asn-Leu-Tyr-OH (I) or its esters, amides, acylated derivs., or salts, which enhance interleukin-1 formation, enhance antibody formation, activate colony-stimulating factor, inhibit pyrexia, reduce PGE2 formation (no data), and are useful as anti-infective, anti-inflammatory, and immunostimulating agents, are prepd. Na-tert-Butoxycarbonyl-O-(bromobenzyloxycarbonyl)-L-tyrosine immobilized to resin support was successively coupled with protected amino acids and deprotected in a usual manner to give I.CF3CO2H, which strongly enhanced Con A-induced thymus cell division. .
Synthetic studies toward 3-amino-6-hydroxy-2-piperidone (AHP)-containing cyclic depsipeptides
Synthetic studies toward 3-amino-6-hydroxy-2-piperidone (AHP)-containing cyclic depsipeptides. Yokokawa, Fumiaki; Inaizumi, Akiko; Shioiri, Takayuki (Graduate School of Pharmaceutical Sciences, Nagoya City University, Nagoya 467-8603, Japan). Peptide Science, Volume Date 2001, 38th, 33-36 (English) 2002 Japanese Peptide Society. CODEN: PSCIFQ. ISSN: 1344-7661. DOCUMENT TYPE: Journal CA Section: 34 (Amino Acids, Peptides, and Proteins) A symposium report. Micropeptin T-20, a representative macrocyclic depsipeptide having 3-amino-6-hydroxy-2-piperidone (Ahp) and exhibiting strong inhibition against chymotrypsin, has been synthesized as its proposed structure by the fragment coupling approach. The unique side chain glyceric acid 3'-O-phosphate was incorporated after the construction of the 19-membered cyclic depsipeptide. 30924-93-7 which is the cas registry number of one of substances is just one of reagents here. The formation of the Ahp nucleus was accomplished almost at the final stage by oxidn. of the alc. with IBX (1-hydroxy-1,2-benziodoxo-3(1H)-one 1-oxide) followed by treatment with TBAF (tetrabutylammonium fluoride). The synthesized micropeptin T-20 was, however, not identical with the natural one, and hence the conclusive evidence on abs. 30924-93-7 which is the cas registry number of one of substances is just one of reagents here. stereochem. of micropeptin T-20 has to await re-isolation and further structural investigations. ..
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