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(R)-α-<<(1,1-dimethylethoxy)carbonyl>amino>-N-methoxy-N-metyl<1,1'-biphenyl>-4-propanamide is a complex chemical compound belonging to the class of biphenyls, characterized by two benzene rings connected by a single covalent bond. This chiral molecule features a carbonyl group, an amino group, a methoxy group, and a methyl group, with the (R)-enantiomer being the biologically active form. Its intricate structure and properties make it a promising candidate for various applications, particularly in the pharmaceutical industry.

162972-36-3

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162972-36-3 Usage

Uses

Used in Pharmaceutical Industry:
(R)-α-<<(1,1-dimethylethoxy)carbonyl>amino>-N-methoxy-N-metyl<1,1'-biphenyl>-4-propanamide is used as a key component in the development of new drugs for various therapeutic applications. Its unique structure and chirality allow for the creation of targeted medications with enhanced efficacy and reduced side effects.
Used in Drug Synthesis:
In the field of medicinal chemistry, (R)-α-<<(1,1-dimethylethoxy)carbonyl>amino>-N-methoxy-N-metyl<1,1'-biphenyl>-4-propanamide serves as an essential building block for the synthesis of more complex and potent pharmaceutical compounds. Its versatile functional groups enable chemists to create a wide range of derivatives with specific biological activities.
Used in Chiral Drug Development:
The (R)-enantiomer of (R)-α-<<(1,1-dimethylethoxy)carbonyl>amino>-N-methoxy-N-metyl<1,1'-biphenyl>-4-propanamide is particularly valuable in the development of chiral drugs, where the stereochemistry of a molecule plays a crucial role in its biological activity. (R)-α-<<(1,1-dimethylethoxy)carbonyl>amino>-N-methoxy-N-metyl<1,1'-biphenyl>-4-propanamide can be utilized to create enantiomerically pure drugs with improved safety and efficacy profiles.
Used in Research and Development:
(R)-α-<<(1,1-dimethylethoxy)carbonyl>amino>-N-methoxy-N-metyl<1,1'-biphenyl>-4-propanamide is also employed as a research tool in the study of biological processes and the development of novel therapeutic strategies. Its unique properties make it an ideal candidate for investigating the interactions between small molecules and biological targets, such as proteins and enzymes.

Check Digit Verification of cas no

The CAS Registry Mumber 162972-36-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,2,9,7 and 2 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 162972-36:
(8*1)+(7*6)+(6*2)+(5*9)+(4*7)+(3*2)+(2*3)+(1*6)=153
153 % 10 = 3
So 162972-36-3 is a valid CAS Registry Number.

162972-36-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (R)-α-<<(1,1-dimethylethoxy)carbonyl>amino>-N-methoxy-N-metyl<1,1'-biphenyl>-4-propanamide

1.2 Other means of identification

Product number -
Other names tert-butyl (R)-(3-([1,1'-biphenyl]-4-yl)-1-(methoxy(methyl)amino)-1-oxopropan-2-yl)carbamate

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:162972-36-3 SDS

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