Welcome to LookChem.com Sign In|Join Free

CAS

  • or

5443-52-7

Post Buying Request

5443-52-7 Suppliers

Recommended suppliersmore

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

5443-52-7 Usage

Chemical Category

2-(methylamino)-4-phenylbutanoic acid belongs to the category of amino acids.

Molecular Weight

The molecular weight of 2-(methylamino)-4-phenylbutanoic acid is 193.24 g/mol.

Physical Appearance

2-(methylamino)-4-phenylbutanoic acid is a white crystalline powder.

Melting Point

The melting point of 2-(methylamino)-4-phenylbutanoic acid is 145-147°C.

Use in Synthesis

2-(methylamino)-4-phenylbutanoic acid is an important intermediate in the synthesis of pharmaceuticals and can be used as a building block for the production of various drugs.

Role in Medicinal Chemistry

This chemical is commonly used in medicinal chemistry and drug development processes due to its role as a precursor in the synthesis of biologically active molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 5443-52-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,4 and 3 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5443-52:
(6*5)+(5*4)+(4*4)+(3*3)+(2*5)+(1*2)=87
87 % 10 = 7
So 5443-52-7 is a valid CAS Registry Number.

5443-52-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(methylamino)-4-phenylbutanoic acid

1.2 Other means of identification

Product number -
Other names -

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:5443-52-7 SDS

5443-52-7Relevant articles and documents

Biocatalytic Synthesis of Chiral N-Functionalized Amino Acids

Hyslop, Julia F.,Lovelock, Sarah L.,Sutton, Peter W.,Brown, Kristin K.,Watson, Allan J. B.,Roiban, Gheorghe-Doru

supporting information, p. 13821 - 13824 (2018/09/27)

N-Functionalized amino acids are important building blocks for the preparation of diverse bioactive molecules, including peptides. The development of sustainable manufacturing routes to chiral N-alkylated amino acids remains a significant challenge in the pharmaceutical and fine-chemical industries. Herein we report the discovery of a structurally diverse panel of biocatalysts which catalyze the asymmetric synthesis of N-alkyl amino acids through the reductive coupling of ketones and amines. Reactions have been performed on a gram scale to yield optically pure N-alkyl-functionalized products in high yields.

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 5443-52-7