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(1S)-(-)-Camphanic acid amide, also known as (-)-eucamide, is an organic compound derived from camphanic acid. It is characterized by its white crystalline solid form, which is insoluble in water but readily soluble in organic solvents. (1S)-(-)-Camphanic acid amide is recognized for its potential in chiral separation and asymmetric synthesis, making it a valuable building block for the synthesis of other organic compounds. Furthermore, (1S)-(-)-Camphanic acid amide has garnered interest for its potential biological activities, such as antimicrobial and anti-inflammatory properties, which contribute to its diverse applications in both industrial and research settings.

54200-37-2

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54200-37-2 Usage

Uses

Used in Chiral Separation and Asymmetric Synthesis:
(1S)-(-)-Camphanic acid amide is utilized as a chiral resolving agent in the separation of enantiomers, which is crucial for the production of pharmaceuticals and other chiral compounds. Its unique stereochemistry allows for the selective interaction with other chiral molecules, facilitating the separation process.
Used in Organic Synthesis:
As a building block, (1S)-(-)-Camphanic acid amide is employed in the synthesis of a variety of organic compounds, contributing to the development of new chemical entities with potential applications in various fields.
Used in Pharmaceutical Industry:
(1S)-(-)-Camphanic acid amide is used as a precursor in the synthesis of pharmaceuticals, leveraging its reactivity and chiral properties to create new drugs with improved efficacy and selectivity.
Used in Antimicrobial Applications:
Due to its antimicrobial properties, (1S)-(-)-Camphanic acid amide is used as an active ingredient in antimicrobial formulations, helping to combat bacterial infections and contributing to the development of new antimicrobial agents.
Used in Anti-Inflammatory Applications:
(1S)-(-)-Camphanic acid amide is applied in anti-inflammatory formulations, taking advantage of its potential to reduce inflammation and alleviate symptoms associated with inflammatory conditions.
Overall, (1S)-(-)-Camphanic acid amide's versatility in chemical and biological properties positions it as a valuable compound across multiple industries, including pharmaceuticals, materials science, and chemical research.

Check Digit Verification of cas no

The CAS Registry Mumber 54200-37-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,2,0 and 0 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 54200-37:
(7*5)+(6*4)+(5*2)+(4*0)+(3*0)+(2*3)+(1*7)=82
82 % 10 = 2
So 54200-37-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H15NO3/c1-8(2)9(3)4-5-10(8,6(11)12)14-7(9)13/h4-5H2,1-3H3,(H2,11,12)/t9-,10+/m0/s1

54200-37-2SDS

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 (1S)-(-)-CAMPHANIC ACID AMIDE

1.2 Other means of identification

Product number -
Other names 4,7,7-Trimethyl-3-oxo-2-oxa-norbornan-1-carbonsaeure-amid

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:54200-37-2 SDS

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