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Detail of "84677-06-5"

  • CAS Number:
  • 84677-06-5
  • Name:
  • Cyclopropanecarboxylicacid, 1-[[(phenylmethoxy)carbonyl]amino]-

  • Superlist Name:
  • 1-(Cbz-amino)cyclopropanecarboxylic acid
  • Molecular Structure:
  • Formula:
  • C12H13 N O4
  • Molecular Weight:
  • 235.24
  • Synonyms:
  • 1-Benzyloxycarbonylaminocyclopropanecarboxylicacid; 1-[[(Phenylmethoxy)carbonyl]amino]cyclopropanecarboxylic acid;N-Benzyloxycarbonyl-1-aminocyclopropanecarboxylic acid
  • Hazard Symbols:
  • Risk Codes:
  • R36/37/38   
  • Safety:
  • S26;S36 Details

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CAS No.84677-06-5 1-(Cbz-amino)cyclopropanecarboxylic acid

Z-1-Aminocyclopropane-1-carboxylic acid

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CAS No.84677-06-5 1-(Cbz-amino)cyclopropanecarboxylic acid

Z-1-Aminocyclopropane-1-carboxylic acid

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CAS No.84677-06-5 1-(Cbz-amino)cyclopropanecarboxylic acid

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CAS No.84677-06-5 1-(Cbz-amino)cyclopropanecarboxylic acid

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CAS No.84677-06-5 1-(Cbz-amino)cyclopropanecarboxylic acid

Z-1-Aminocyclopropane-1-carboxylic acid

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CAS No.84677-06-5 1-(Cbz-amino)cyclopropanecarboxylic acid

Assay:99%

Supplier:shanghai jinshan pharmaceutical Co.,Ltd [ China (Mainland)]

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CAS No.84677-06-5 1-(Cbz-amino)cyclopropanecarboxylic acid

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CAS No.84677-06-5 1-(Cbz-amino)cyclopropanecarboxylic acid

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CAS No.84677-06-5 1-(Cbz-amino)cyclopropanecarboxylic acid

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CAS No.84677-06-5 1-(Cbz-amino)cyclopropanecarboxylic acid

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CAS No.84677-06-5 1-(Cbz-amino)cyclopropanecarboxylic acid

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CAS No.84677-06-5 1-(Cbz-amino)cyclopropanecarboxylic acid

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CAS No.84677-06-5 1-(Cbz-amino)cyclopropanecarboxylic acid

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CAS No.84677-06-5 1-(Cbz-amino)cyclopropanecarboxylic acid

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CAS No.84677-06-5 1-(Cbz-amino)cyclopropanecarboxylic acid

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Reference

Two analogs of oxytocin with modified proline cyclic structure
Two analogs of oxytocin with modified proline cyclic structure. Prochazka, Zdenko; Lebl, Michal; Barth, Tomislav; Hlavacek, Jan; Jost, Karel (Inst. Org. Chem. Biochem., Slovak Acad. Sci., Prague 166 10/6, Czech.). Pept., Proc. Eur. Pept. Symp. 88463-33-6 and 84677-06-5 which are cas registry numbers are also used here., 17th, Meeting Date 1982, 441-4. Edited by: Blaha, Karel; Malon, Petr. de Gruyter: Berlin, Fed. Rep. Ger. (English) 1983. CODEN: 50GFAA. DOCUMENT TYPE: Conference CA Section: 34 (Amino Acids, Peptides, and Proteins) Section cross-reference(s): 1 Oxytocin analogs I and II were prepd. by condensation of protected hexapeptide acid with carboxy terminal peptides. Both I and II have lower biolog. activities than oxytocin. .
Convenient synthesis and isolation of 1-aminocyclopropane-1-carboxylic acid (ACC) and N-protected ACC derivatives
Convenient synthesis and isolation of 1-aminocyclopropane-1-carboxylic acid (ACC) and N-protected ACC derivatives. Allwein, Shawn P.; Secord, Elizabeth A.; Martins, Andrew; Mitten, Jeffrey V. 84677-06-5 and 383-63-1 are cas registry numbers. These chemicals are also mentioned in this article.; Nelson, Todd D.; Kress, Michael H.; Dolling, H. (Department of Process Research, Merck Research Laboratories, Wayne, PA 19087, USA). Synlett, (14), 2489-2492 (English) 2004 Georg Thieme Verlag. CODEN: SYNLES. ISSN: 0936-5214. DOCUMENT TYPE: Journal CA Section: 34 (Amino Acids, Peptides, and Proteins) A convenient route to 1-aminocyclopropane-1-carboxylic acid (ACC) and N-protected derivs. was developed. This route utilizes a bis-alkylation of an O-benzyl glycine derived imine followed by global deprotection via hydrogenation. Direct isolation of ACC from a non-aq. stream or efficient conversion to N-protected derivs. in a single flask is described. .
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