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BOC-(R)-3-AMINO-5-PHENYLPENTANOIC ACID, also known as Boc-D-(R)-ap5-OH, is a chemical compound with the formula C16H23NO4. It is a white to off-white crystalline powder with a molecular weight of 289.36 g/mol. BOC-(R)-3-AMINO-5-PHENYLPENTANOIC ACID is a derivative of the amino acid leucine, featuring a Boc (tert-butyloxycarbonyl) protecting group attached to the amino group. It serves as a versatile building block in the synthesis of various pharmaceuticals and organic compounds, particularly in peptide synthesis and as a chiral building block in organic chemistry.

218608-83-4

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218608-83-4 Usage

Uses

Used in Pharmaceutical Synthesis:
BOC-(R)-3-AMINO-5-PHENYLPENTANOIC ACID is used as a building block for the synthesis of various pharmaceuticals. Its unique structure and the presence of the Boc protecting group make it suitable for the development of new drugs with specific therapeutic properties.
Used in Peptide Synthesis:
In peptide synthesis, BOC-(R)-3-AMINO-5-PHENYLPENTANOIC ACID is used as a chiral building block. The Boc protecting group allows for selective deprotection and coupling reactions, facilitating the synthesis of complex peptide sequences with high stereoselectivity.
Used in Organic Chemistry:
BOC-(R)-3-AMINO-5-PHENYLPENTANOIC ACID is employed as a chiral building block in organic chemistry. Its unique structure and the Boc protecting group enable the synthesis of various organic compounds with specific stereochemistry, which is crucial for the development of enantioselective reactions and the production of chiral molecules with desired biological activities.
Used in Research and Development:
BOC-(R)-3-AMINO-5-PHENYLPENTANOIC ACID is utilized in research and development for the exploration of new synthetic routes, the discovery of novel compounds, and the investigation of the structure-activity relationships of various pharmaceuticals and organic compounds. Its unique properties and the presence of the Boc protecting group make it a valuable tool for chemists in the design and synthesis of new molecules with potential applications in various fields.

Check Digit Verification of cas no

The CAS Registry Mumber 218608-83-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,8,6,0 and 8 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 218608-83:
(8*2)+(7*1)+(6*8)+(5*6)+(4*0)+(3*8)+(2*8)+(1*3)=144
144 % 10 = 4
So 218608-83-4 is a valid CAS Registry Number.
InChI:InChI=1/C16H23NO4/c1-16(2,3)21-15(20)17-13(11-14(18)19)10-9-12-7-5-4-6-8-12/h4-8,13H,9-11H2,1-3H3,(H,17,20)(H,18,19)/t13-/m1/s1

218608-83-4 Well-known Company Product Price

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  • Alfa Aesar

  • (H52055)  (R)-3-(Boc-amino)-5-phenylpentanoic acid, 95%   

  • 218608-83-4

  • 250mg

  • 882.0CNY

  • Detail
  • Alfa Aesar

  • (H52055)  (R)-3-(Boc-amino)-5-phenylpentanoic acid, 95%   

  • 218608-83-4

  • 1g

  • 2822.0CNY

  • Detail
  • Aldrich

  • (78018)  (R)-3-(Boc-amino)-5-phenylpentanoicacid  ≥97.0% (HPLC)

  • 218608-83-4

  • 78018-500MG-F

  • 2,116.53CNY

  • Detail

218608-83-4Upstream product

218608-83-4Relevant academic research and scientific papers

Efflux pump inhibitors

-

, (2008/06/13)

Compounds are described which have efflux pump inhibitor activity. Also described are methods of using such efflux pump inhibitor compounds and pharmaceutical compositions which include such compounds.

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