Welcome to LookChem.com Sign In|Join Free
  • or
N-Boc-(S)-2-amino-2-(3-chlorophenyl)acetic acid is a chemical compound characterized by the presence of a Boc (tert-butyloxycarbonyl) protecting group on the nitrogen atom and an (S)-configuration at the chiral center. It is derived from 2-amino-2-(3-chlorophenyl)acetic acid, which is known for its anti-inflammatory properties. N-Boc-(S)-2-amino-2-(3-chlorophenyl)acetic acid holds potential in the fields of medicinal chemistry and drug development, serving as a valuable building block for the synthesis of pharmaceuticals or as a research tool for studying biochemical pathways and receptors. The Boc group can be removed under mild conditions, enabling the release of the free amine for further chemical reactions or biological studies. Its distinctive structural attributes make it a promising candidate for the design and development of innovative bioactive molecules.

1217643-80-5

Post Buying Request

1217643-80-5 Suppliers

Recommended suppliers

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

1217643-80-5 Usage

Uses

Used in Medicinal Chemistry:
N-Boc-(S)-2-amino-2-(3-chlorophenyl)acetic acid is utilized as a key intermediate in the synthesis of various pharmaceuticals, particularly those with anti-inflammatory properties. Its Boc protecting group allows for controlled deprotection, facilitating the synthesis of complex molecular structures.
Used in Drug Development:
In the pharmaceutical industry, N-Boc-(S)-2-amino-2-(3-chlorophenyl)acetic acid serves as a building block for the development of novel drugs. Its unique structural features and the ability to remove the Boc group under mild conditions make it an attractive candidate for the creation of bioactive molecules with potential therapeutic applications.
Used in Research and Development:
N-Boc-(S)-2-amino-2-(3-chlorophenyl)acetic acid is employed as a research tool in the study of biochemical pathways and receptors. Its (S)-configuration and the presence of the Boc protecting group provide a platform for investigating the stereoselectivity and reactivity of various biological processes.
Used in Biochemical Pathway Studies:
N-Boc-(S)-2-amino-2-(3-chlorophenyl)acetic acid is used as a probe in the investigation of enzyme mechanisms and substrate specificities, particularly in the context of enzymes that act on chiral centers. Its unique structural features allow researchers to gain insights into the selectivity and efficiency of enzymatic reactions.
Used in Receptor Binding Studies:
N-Boc-(S)-2-amino-2-(3-chlorophenyl)acetic acid is utilized in the study of receptor-ligand interactions, providing valuable information on the binding preferences and selectivity of various receptors. This knowledge can be instrumental in the design of drugs with improved targeting and efficacy.

Check Digit Verification of cas no

The CAS Registry Mumber 1217643-80-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,7,6,4 and 3 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1217643-80:
(9*1)+(8*2)+(7*1)+(6*7)+(5*6)+(4*4)+(3*3)+(2*8)+(1*0)=145
145 % 10 = 5
So 1217643-80-5 is a valid CAS Registry Number.

1217643-80-5SDS

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 (2S)-2-(3-chlorophenyl)-2-[(2-methylpropan-2-yl)oxycarbonylamino]acetic acid

1.2 Other means of identification

Product number -
Other names N-Boc-2-(3'-Chlorophenyl)-L-glycine

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:1217643-80-5 SDS

1217643-80-5Upstream product

1217643-80-5Downstream Products

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 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 1217643-80-5