Welcome to LookChem.com Sign In|Join Free

CAS

  • or

193693-60-6

Post Buying Request

193693-60-6 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

193693-60-6 Usage

Description

Fmoc-L-beta-homoproline, also known as N-(9-fluorenylmethoxycarbonyl)-L-beta-homoproline, is a synthetic, non-natural amino acid derivative. It is a white to off-white powder and is widely used in various industries due to its unique chemical properties and reactivity.

Uses

Fmoc-L-beta-homoproline is used as an important organic intermediate in the fields of agrochemicals, pharmaceuticals, and dyestuff. Its application in these industries is primarily due to its ability to enhance the properties and performance of the final products.
Used in Pharmaceutical Industry:
Fmoc-L-beta-homoproline is used as a building block in peptide synthesis, allowing for the creation of complex and specific peptide sequences. This is crucial for the development of new drugs and therapeutic agents, as peptides can be tailored to target specific biological pathways and receptors.
Used in Drug Screening:
In the drug screening process, Fmoc-L-beta-homoproline is utilized to create a diverse library of peptide-based compounds. These compounds can then be screened for potential biological activity, leading to the discovery of new drug candidates with specific therapeutic properties.
Used in Agrochemical Industry:
Fmoc-L-beta-homoproline is employed as an intermediate in the synthesis of various agrochemicals, such as pesticides and herbicides. Its incorporation can improve the effectiveness and selectivity of these chemicals, leading to more efficient and environmentally friendly products.
Used in Dyestuff Industry:
In the dyestuff industry, Fmoc-L-beta-homoproline is used to synthesize novel dyes with unique color properties and improved stability. This allows for the development of new and innovative colorants for various applications, such as textiles, plastics, and printing inks.

Check Digit Verification of cas no

The CAS Registry Mumber 193693-60-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,3,6,9 and 3 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 193693-60:
(8*1)+(7*9)+(6*3)+(5*6)+(4*9)+(3*3)+(2*6)+(1*0)=176
176 % 10 = 6
So 193693-60-6 is a valid CAS Registry Number.
InChI:InChI=1/C21H21NO4/c23-20(24)12-14-6-5-11-22(14)21(25)26-13-19-17-9-3-1-7-15(17)16-8-2-4-10-18(16)19/h1-4,7-10,14,19H,5-6,11-13H2,(H,23,24)/t14-/m0/s1

193693-60-6 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Alfa Aesar

  • (H52060)  N-Fmoc-L-beta-homoproline, 95%   

  • 193693-60-6

  • 250mg

  • 882.0CNY

  • Detail
  • Alfa Aesar

  • (H52060)  N-Fmoc-L-beta-homoproline, 95%   

  • 193693-60-6

  • 1g

  • 2822.0CNY

  • Detail
  • Aldrich

  • (47912)  Fmoc-L3-homoproline  ≥98.0% (HPLC)

  • 193693-60-6

  • 47912-1G

  • 4,626.18CNY

  • Detail

193693-60-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name Fmoc-L-beta-homoproline

1.2 Other means of identification

Product number -
Other names 2-[(2S)-1-(9H-fluoren-9-ylmethoxycarbonyl)pyrrolidin-2-yl]acetic 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:193693-60-6 SDS

193693-60-6Relevant articles and documents

Synthesis of N-{[(9H-Fluoren-9-yl)methoxy]carbonyl}-Protected (Fmoc) β-Amino Acids (= Homo-α-Amino Acids) by Direct Homologation

Ellmerer-Mueller, Ernst P.,Broessner, Dagmar,Maslouh, Najib,Tako, Andreas

, p. 59 - 65 (1998)

The successful application of the Arndt-Eistert protocol starting from commercially available N-{[(9H-fluoren-9-yl)methoxy]carbonyl}-protected (Fmoc) α-amino acids leading to enantiomerically pure N-Fmoc-Protected β-amino acids in only two steps and with high yield is reported.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 193693-60-6