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CAS

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84799-87-1

enalaprilate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 84799-87-1 Structure

  • Basic information

    1. Product Name: enalaprilate
    2. Synonyms: enalaprilate
    3. CAS NO:84799-87-1
    4. Molecular Formula:
    5. Molecular Weight: 348.399
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 84799-87-1.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: enalaprilate(CAS DataBase Reference)
    10. NIST Chemistry Reference: enalaprilate(84799-87-1)
    11. EPA Substance Registry System: enalaprilate(84799-87-1)

  • 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: 84799-87-1(Hazardous Substances Data)

84799-87-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 84799-87-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,7,9 and 9 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 84799-87:
(7*8)+(6*4)+(5*7)+(4*9)+(3*9)+(2*8)+(1*7)=201
201 % 10 = 1
So 84799-87-1 is a valid CAS Registry Number.

84799-87-1Downstream Products

84799-87-1Relevant articles and documents

Synthesis of N-(1-carboxy-3-phenylpropen-2-yl)alanylproline

Slavinskaya,Chipens,Katkevich,Sile,Korchagova,Grigor'eva,Lukevits

, p. 405 - 407 (1996)

A method has been developed for the synthesis of N-(1-carboxy-3-phenylpropen-2-yl)alanylproline by reductive alkylation of alanylproline by the sodium salt of 2-oxo-4-phenylbutertoic acid, using sodium cyanoborohydride and sodium borohydride as reducing agents. The products were separated chromatographically, Under the conditions of the reaction, sodium borohydride in a neutral medium preferentially reduces the double bond of the Schiff base. Sodium cyanoborohydride reduces, in addition, the double bond of the 2-oxo-4-phenylbutenoic acid, forming enalaprilate. 1996 Plenum Publishing Corporation.

ANTIHYPERTENSIVE COMPOSITION

-

, (2008/06/13)

A pharmaceutical composition is disclosed which comprises the combination of interphenylene 9-thia-11-oxo-12-aza prostanoic acid derivatives and carboxyalkyl dipeptide derivatives.

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