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BOC-(S)-ALPHA-BENZYL-PROLINE is a chemical compound that belongs to the class of proline derivatives. It is characterized by the presence of a BOC (tert-butoxycarbonyl) protective group and an alpha-benzyl substituent attached to the proline molecule. BOC-(S)-ALPHA-BENZYL-PROLINE is widely recognized for its role in organic synthesis and pharmaceutical research due to its diverse biological activities and potential therapeutic applications. Its unique stereochemistry and functional groups make it a valuable asset in the design of new molecules with enhanced pharmacological properties, thereby playing a pivotal role in the development of novel drugs and chemical entities with potential medical benefits.

706806-61-3

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706806-61-3 Usage

Uses

Used in Pharmaceutical Research and Development:
BOC-(S)-ALPHA-BENZYL-PROLINE is used as a chiral building block for the synthesis of various drug candidates and bioactive compounds. Its specific stereochemistry and functional groups contribute to the development of molecules with improved pharmacological properties, making it an essential component in the creation of innovative medications.
Used in Organic Synthesis:
In the field of organic synthesis, BOC-(S)-ALPHA-BENZYL-PROLINE serves as a key intermediate for the preparation of complex organic molecules. Its unique structure allows for versatile reactions and transformations, facilitating the synthesis of a wide range of chemical entities with potential applications in various industries.
Used in Medicinal Chemistry:
BOC-(S)-ALPHA-BENZYL-PROLINE is utilized in medicinal chemistry for the design and optimization of drug molecules. Its presence in a compound can influence the pharmacokinetics, pharmacodynamics, and overall efficacy of a drug, making it a valuable tool in the development of new therapeutic agents.
Used in the Development of Bioactive Compounds:
This proline derivative is also employed in the synthesis of bioactive compounds with potential applications in various therapeutic areas. Its unique structural features enable the creation of molecules with specific biological activities, contributing to the advancement of treatments for various diseases and conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 706806-61-3 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 1 respectively.
Calculate Digit Verification of CAS Registry Number 706806-61:
(8*7)+(7*0)+(6*6)+(5*8)+(4*0)+(3*6)+(2*6)+(1*1)=163
163 % 10 = 3
So 706806-61-3 is a valid CAS Registry Number.
InChI:InChI=1/C17H23NO4/c1-16(2,3)22-15(21)18-11-7-10-17(18,14(19)20)12-13-8-5-4-6-9-13/h4-6,8-9H,7,10-12H2,1-3H3,(H,19,20)/t17-/m0/s1

706806-61-3 Well-known Company Product Price

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  • (Code)Product description
  • CAS number
  • Packaging
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  • Alfa Aesar

  • (H52186)  2-Benzyl-N-Boc-D-proline, 95%   

  • 706806-61-3

  • 250mg

  • 1548.0CNY

  • Detail
  • Alfa Aesar

  • (H52186)  2-Benzyl-N-Boc-D-proline, 95%   

  • 706806-61-3

  • 1g

  • 4939.0CNY

  • Detail
  • Aldrich

  • (76896)  Boc-(S)-α-benzyl-Pro-OH  ≥97.0%

  • 706806-61-3

  • 76896-500MG-F

  • 4,504.50CNY

  • Detail

706806-61-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S)-2-benzyl-1-[(2-methylpropan-2-yl)oxycarbonyl]pyrrolidine-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names Boc-|A-benzyl-D-proline

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:706806-61-3 SDS

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