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N-(4-fluorophenyl)-N-(2-carboxyphenyl)glycin is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 180911-99-3 Structure
  • Basic information

    1. Product Name: N-(4-fluorophenyl)-N-(2-carboxyphenyl)glycin
    2. Synonyms: N-(4-fluorophenyl)-N-(2-carboxyphenyl)glycin
    3. CAS NO:180911-99-3
    4. Molecular Formula:
    5. Molecular Weight: 289.263
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 180911-99-3.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-(4-fluorophenyl)-N-(2-carboxyphenyl)glycin(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-(4-fluorophenyl)-N-(2-carboxyphenyl)glycin(180911-99-3)
    11. EPA Substance Registry System: N-(4-fluorophenyl)-N-(2-carboxyphenyl)glycin(180911-99-3)
  • 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: 180911-99-3(Hazardous Substances Data)

180911-99-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 180911-99-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,0,9,1 and 1 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 180911-99:
(8*1)+(7*8)+(6*0)+(5*9)+(4*1)+(3*1)+(2*9)+(1*9)=143
143 % 10 = 3
So 180911-99-3 is a valid CAS Registry Number.

180911-99-3Relevant articles and documents

Process for the preparation of 5-chloro-1-(4-fluorophenyl)-3-(1,2,3,6-tetrahydropyridin-4-yl)indole and method of manufacturing sertindole

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Example 1, (2010/01/31)

A process of manufacturing sertindole comprising reacting 5-chloro-1-(4-fluorophenyl)indole with 4-piperidone in a mixture of an acetic acid and concentrated HCl; reduction of the resulting 5-chloro-1-(4-fluorophenyl)-3-(1,2,3,6-tetrahydropyridin-4-yl)indole and reaction of this compound with 1-(2-chloroethyl)-2-imidazolidinon in order to obtain sertindole.

Structure-activity relationships of a series of novel (piperazinylbutyl)thiazolidinone antipsychotic agents related to 3-[4-[4-(6- fluorobenzo[b]thien-3-yl)-1-piperazinyl]butyl]-2,5,5-trimethyl-4- thiazolidinone maleate

Hrib, Nicholas J.,Jurcak, John G.,Bregna, Deborah E.,Burgher, Kendra L.,Hartman, Harold B.,Kafka, Sharon,Kerman, Lisa L.,Kongsamut, Sam,Roehr, Joachim E.,Szewczak, Mark R.,Woods-Kettelberger, Ann T.,Corbett, Roy

, p. 4044 - 4057 (2007/10/03)

HP-236 (3-[4-[4-(6-Fluorobenzo[b]thien-3-yl)-1-piperazinyl]butyl]- 2,5,5-trimethyl-4-thiazolidinone maleate; P-9236) (54) displayed a pharmacological profile indicative of potential atypical antipsychotic activity. A series of piperazinyl butyl thiazolidi

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