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BOC-(R)-ALPHA-(3-CHLOROBENZYL)-PROLINE is a chemical compound derived from proline, an essential amino acid crucial for protein structure and function. BOC-(R)-ALPHA-(3-CHLOROBENZYL)-PROLINE features a BOC (tert-butyloxycarbonyl) protecting group, which is commonly utilized in peptide synthesis to prevent unwanted reactions. Additionally, the (R)-alpha-(3-chlorobenzyl) group provides a specific functional moiety for further chemical modifications. It plays a significant role in medicinal chemistry, particularly in the development of new drugs and therapeutic agents.

706806-68-0

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706806-68-0 Usage

Uses

Used in Pharmaceutical Industry:
BOC-(R)-ALPHA-(3-CHLOROBENZYL)-PROLINE is used as a key intermediate in the synthesis of peptides and pharmaceuticals for its ability to facilitate the creation of complex molecular structures with specific functionalities. The protecting BOC group ensures that the molecule can be selectively modified without affecting other parts of the peptide chain, which is vital for the development of targeted drug therapies.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, BOC-(R)-ALPHA-(3-CHLOROBENZYL)-PROLINE serves as a valuable building block for the design and synthesis of novel drug candidates. Its unique structural features allow researchers to explore new avenues in drug discovery, potentially leading to the creation of more effective and selective treatments for various diseases and conditions.
Used in Peptide Synthesis:
BOC-(R)-ALPHA-(3-CHLOROBENZYL)-PROLINE is utilized as a protected amino acid in peptide synthesis, where the BOC group shields the amino and carboxyl groups from unwanted side reactions during the assembly of peptide chains. This protection is crucial for the successful synthesis of peptides with specific sequences and functions, which can be further used in biological and medical applications.
Overall, BOC-(R)-ALPHA-(3-CHLOROBENZYL)-PROLINE is a versatile compound with applications across various sectors of the pharmaceutical and chemical industries, contributing to the advancement of drug development and the understanding of peptide chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 706806-68-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,0,6,8,0 and 6 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 706806-68:
(8*7)+(7*0)+(6*6)+(5*8)+(4*0)+(3*6)+(2*6)+(1*8)=170
170 % 10 = 0
So 706806-68-0 is a valid CAS Registry Number.
InChI:InChI=1/C17H22ClNO4/c1-16(2,3)23-15(22)19-9-5-8-17(19,14(20)21)11-12-6-4-7-13(18)10-12/h4,6-7,10H,5,8-9,11H2,1-3H3,(H,20,21)/t17-/m1/s1

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