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(R)-(+)-N-(1-PHENYLETHYL)PHTHALAMIC ACID is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

21752-35-2

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21752-35-2 Usage

Uses

Acid for the resolution of amines.

Check Digit Verification of cas no

The CAS Registry Mumber 21752-35-2 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 5 respectively.
Calculate Digit Verification of CAS Registry Number 21752-35:
(7*2)+(6*1)+(5*7)+(4*5)+(3*2)+(2*3)+(1*5)=92
92 % 10 = 2
So 21752-35-2 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-/m1/s1

21752-35-2 Well-known Company Product Price

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  • TCI America

  • (M1622)  (R)-(+)-N-(α-Methylbenzyl)phthalamic Acid  >98.0%(HPLC)(T)

  • 21752-35-2

  • 1g

  • 460.00CNY

  • Detail

  • TCI America

  • (M1622)  (R)-(+)-N-(α-Methylbenzyl)phthalamic Acid  >98.0%(HPLC)(T)

  • 21752-35-2

  • 5g

  • 1,560.00CNY

  • Detail

  • Aldrich

  • (461458)  (R)-(+)-N-(1-Phenylethyl)phthalamicacid  97%

  • 21752-35-2

  • 461458-1G

  • 586.17CNY

  • Detail

21752-35-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[[(1R)-1-phenylethyl]carbamoyl]benzoic acid

1.2 Other means of identification

Product number -
Other names (R)-2-((1-Phenylethyl)carbamoyl)benzoic acid

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:21752-35-2 SDS

21752-35-2Relevant academic research and scientific papers

METHOD OF PREPARING (3R,4S)-3-ACETAMIDO-4-ALLYL-N-(TERT-BUTYL)PYRROLIDINE-3-CARBOXAMIDE

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Paragraph 0171; 0172, (2019/01/04)

A method is provided to conveniently separate racemic (3R,4S)-3-acetamido-4-allyl-N-(tert-butyl)pyrrolidine-3-carboxamide and (3S,4R)-3-acetamido-4-allyl-N-(tert-butyl)pyrrolidine-3-carboxamide using selective crystallization with chiral carboxylic acids.

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.

Use of MDL-100,907 for treatment of allergic and eosinophil mediated diseases

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Page/Page column 10; 11, (2010/10/20)

Methods of modulating eosinophil migration, chemotaxis or generation, in vitro, ex vivo, and in vivo are provided. Methods include contacting eosinophils with an amount of 5-HT2A receptor agonist or antagonist sufficient to modulate eosinophil migration, chemotaxis or generation.

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