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(R)-4-(FMOC-AMINO)-5-PHENYLPENTANOIC ACI is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

269078-74-2

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269078-74-2 Usage

Uses

Fmoc-(R)-4-amino-5-phenylpentanoic Acid is a useful synthetic intermediate.

Check Digit Verification of cas no

The CAS Registry Mumber 269078-74-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,9,0,7 and 8 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 269078-74:
(8*2)+(7*6)+(6*9)+(5*0)+(4*7)+(3*8)+(2*7)+(1*4)=182
182 % 10 = 2
So 269078-74-2 is a valid CAS Registry Number.
InChI:InChI=1/C26H25NO4/c28-25(29)15-14-19(16-18-8-2-1-3-9-18)27-26(30)31-17-24-22-12-6-4-10-20(22)21-11-5-7-13-23(21)24/h1-13,19,24H,14-17H2,(H,27,30)(H,28,29)/t19-/m1/s1

269078-74-2 Well-known Company Product Price

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  • Aldrich

  • (93669)  (R)-4-(Fmoc-amino)-5-phenylpentanoicacid  ≥97.0%

  • 269078-74-2

  • 93669-500MG-F

  • 3,125.07CNY

  • Detail

269078-74-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (4R)-4-(9H-fluoren-9-ylmethoxycarbonylamino)-5-phenylpentanoic acid

1.2 Other means of identification

Product number -
Other names Fmoc-(R)-4-amino-5-phenylpentanoic acid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:269078-74-2 SDS

269078-74-2Relevant academic research and scientific papers

Potent Antimicrobial Activity of Lipidated Short α,γ-Hybrid Peptides

Benke, Sushil N.,Thulasiram, Hirekodathakallu V.,Gopi, Hosahudya N.

, p. 1610 - 1615 (2017/10/16)

Herein we report the potent antimicrobial activity of α,γ-hybrid lipopeptides composed of 1:1 alternating α- and γ-amino acids. Along with their potent antimicrobial activity against various Gram-positive and Gram-negative bacteria, these hybrid lipopepti

Protein secondary structure mimetics: Crystal conformations of α/γ4-hybrid peptide12-helices with proteinogenic side chains and their analogy with α- And β-peptide helices

Jadhav, Sandip V.,Bandyopadhyay, Anupam,Gopi, Hosahudya N.

supporting information, p. 509 - 514 (2013/03/14)

Numerous strategies have been developed to mimic the α-helical secondary structure using hybrid peptides containing non-natural amino acids. In contrast to the β- and α/β-hybrid peptides, very little is known about the folding patterns of hybrid peptides

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