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N-(carboxymethyl)-N-(3-chlorophenyl)Glycine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 125340-66-1 Structure
  • Basic information

    1. Product Name: N-(carboxymethyl)-N-(3-chlorophenyl)Glycine
    2. Synonyms: N-(carboxymethyl)-N-(3-chlorophenyl)Glycine
    3. CAS NO:125340-66-1
    4. Molecular Formula:
    5. Molecular Weight: 0
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 125340-66-1.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: N-(carboxymethyl)-N-(3-chlorophenyl)Glycine(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-(carboxymethyl)-N-(3-chlorophenyl)Glycine(125340-66-1)
    11. EPA Substance Registry System: N-(carboxymethyl)-N-(3-chlorophenyl)Glycine(125340-66-1)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 125340-66-1(Hazardous Substances Data)

125340-66-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 125340-66-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,5,3,4 and 0 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 125340-66:
(8*1)+(7*2)+(6*5)+(5*3)+(4*4)+(3*0)+(2*6)+(1*6)=101
101 % 10 = 1
So 125340-66-1 is a valid CAS Registry Number.

125340-66-1Downstream Products

125340-66-1Relevant articles and documents

Synthesis of Dicarboxylic Acids from Aqueous Solutions of Diols with Hydrogen Evolution Catalyzed by an Iridium Complex

Fujita, Ken-ichi,Toyooka, Genki

, (2020/07/13)

A catalytic system for the synthesis of dicarboxylic acids from aqueous solutions of diols accompanied by the evolution of hydrogen was developed. An iridium complex bearing a functional bipyridonate ligand with N,N-dimethylamino substituents exhibited a high catalytic performance for this type of dehydrogenative reaction. For example, adipic acid was synthesized from an aqueous solution of 1,6-hexanediol in 97 % yield accompanied by the evolution of four equivalents of hydrogen by the present catalytic system. It should be noted that the simultaneous production of industrially important dicarboxylic acids and hydrogen, which is useful as an energy carrier, was achieved. In addition, the selective dehydrogenative oxidation of vicinal diols to give α-hydroxycarboxylic acids was also accomplished.

THERAPEUTIC AGENT FOR CEREBRAL INFARCTION

-

, (2012/08/08)

The invention provides a therapeutic drug for ischemic stroke. The therapeutic drug has the formula (I) wherein each symbol is as defined herein, or a pharmacologically acceptable salt thereof, or a solvate thereof, as an active ingredient.

One-Pot Synthesis of Substituted Aniline-N,N-diacetic Acids

Lin, Shaw-Tao,Huang, Ru-Jiun

, p. 548 - 549 (2007/10/02)

Substituted aniline-N,N-diacetic acids are synthesized by reaction of substituted anilines with n-butyllithium and sodium chloroacetate in good yields.

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