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CAS

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187876-40-0

(S)-3-(5-Iodo-2-methylamino-benzoylamino)-butyric acid ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 187876-40-0 Structure

  • Basic information

    1. Product Name: (S)-3-(5-Iodo-2-methylamino-benzoylamino)-butyric acid ethyl ester
    2. Synonyms: (S)-3-(5-Iodo-2-methylamino-benzoylamino)-butyric acid ethyl ester
    3. CAS NO:187876-40-0
    4. Molecular Formula:
    5. Molecular Weight: 390.221
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 187876-40-0.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: (S)-3-(5-Iodo-2-methylamino-benzoylamino)-butyric acid ethyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: (S)-3-(5-Iodo-2-methylamino-benzoylamino)-butyric acid ethyl ester(187876-40-0)
    11. EPA Substance Registry System: (S)-3-(5-Iodo-2-methylamino-benzoylamino)-butyric acid ethyl ester(187876-40-0)

  • 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: 187876-40-0(Hazardous Substances Data)

187876-40-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 187876-40-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,7,8,7 and 6 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 187876-40:
(8*1)+(7*8)+(6*7)+(5*8)+(4*7)+(3*6)+(2*4)+(1*0)=200
200 % 10 = 0
So 187876-40-0 is a valid CAS Registry Number.

187876-40-0Relevant articles and documents

From peptide to non-peptide. 3. Atropisomerie GPIIbIIIa antagonists containing the 3,4-dihydro-1H-1,4-benzodiazepine-2,5-dione nucleus

Blackburn, Brent K.,Lee, Arthur,Baier, Mark,Kohl, Benjamin,Olivero, Alan G.,Matamoros, Regina,Robarge, Kirk D.,McDowell, Robert S.

, p. 717 - 729 (1997)

The benzodiazepinedione class of non-peptidal GPIIbIIIa antagonists has been modified to allow the isolation of noninterconverting rotational isomers, or atropisomers, with the aim of examining their structure-activity relationships as compared to active

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