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21752-36-3

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21752-36-3 Usage

Description

(S)-(-)-N-(1-PHENYLETHYL)PHTHALAMIC ACID, also known as N-phenylethylphthalamic acid, is a synthetic compound that belongs to the phthalamic acid derivatives. It is recognized for its potential applications in research and industry due to its diverse biological activities. This chiral compound is particularly noted for its use in the resolution of enantiomers and as a building block in the synthesis of specialized chemicals. Additionally, it has garnered interest for its potential antiviral and antibacterial properties, although further research is necessary to elucidate its full spectrum of applications and mechanisms of action.

Uses

Used in Pharmaceutical Research:
(S)-(-)-N-(1-PHENYLETHYL)PHTHALAMIC ACID is used as a chiral resolving agent for the separation of enantiomers, which is crucial in pharmaceutical development where the biological activity of each enantiomer may differ significantly.
Used in Chemical Synthesis:
In the chemical industry, (S)-(-)-N-(1-PHENYLETHYL)PHTHALAMIC ACID serves as a building block for the synthesis of other specialized chemicals, contributing to the creation of novel compounds with specific applications.
Used in Antiviral and Antibacterial Research:
(S)-(-)-N-(1-PHENYLETHYL)PHTHALAMIC ACID is studied for its potential antiviral and antibacterial properties, indicating its possible use in the development of new treatments for viral and bacterial infections. Further research is required to confirm its efficacy and safety in these applications.

Check Digit Verification of cas no

The CAS Registry Mumber 21752-36-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,7,5 and 2 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 21752-36:
(7*2)+(6*1)+(5*7)+(4*5)+(3*2)+(2*3)+(1*6)=93
93 % 10 = 3
So 21752-36-3 is a valid CAS Registry Number.
InChI:InChI=1/C16H15NO3/c1-11(12-7-3-2-4-8-12)17-15(18)13-9-5-6-10-14(13)16(19)20/h2-11H,1H3,(H,17,18)(H,19,20)/t11-/m0/s1

21752-36-3 Well-known Company Product Price

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  • TCI America

  • (M0824)  (S)-(-)-N-(α-Methylbenzyl)phthalamic Acid  >98.0%(T)

  • 21752-36-3

  • 1g

  • 490.00CNY

  • Detail
  • Aldrich

  • (461466)  (S)-(−)-N-(1-Phenylethyl)phthalamicacid  97%

  • 21752-36-3

  • 461466-1G

  • 833.04CNY

  • Detail

21752-36-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name (S)-(-)-N-(1-PHENYLETHYL)PHTHALAMIC ACID

1.2 Other means of identification

Product number -
Other names Einecs 244-571-6

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:21752-36-3 SDS

21752-36-3Downstream Products

21752-36-3Relevant articles and documents

PROCESS FOR ENANTIOMERIC ENRICHMENT OF 2 ', 6 ' - PIPECOLOXYLIDIDE

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Page/Page column 17, (2014/02/15)

The invention discloses a process for enantiomeric enrichment of 2',6'-pipecoloxylidide using a chiral carbamoyl benzoic acid to provide (S)-enantiomer in high yield and high enantiomeric purity. The invention also discloses novel intermediates formed in the process of enantiomeric enrichment of 2',6'-pipecoloxylidide, preparation of N- substituted amidic acids and alkylation of 2',6'-pipecoloxylidide.

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