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N--N'-<(2,2,2-trichloroethoxy)carbonyl>-L-alanyl>-L-4-hydroxyproline 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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  • 103654-87-1 Structure
  • Basic information

    1. Product Name: N--N'-<(2,2,2-trichloroethoxy)carbonyl>-L-alanyl>-L-4-hydroxyproline ethyl ester
    2. Synonyms: N--N'-<(2,2,2-trichloroethoxy)carbonyl>-L-alanyl>-L-4-hydroxyproline ethyl ester
    3. CAS NO:103654-87-1
    4. Molecular Formula:
    5. Molecular Weight: 595.905
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 103654-87-1.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: N--N'-<(2,2,2-trichloroethoxy)carbonyl>-L-alanyl>-L-4-hydroxyproline ethyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: N--N'-<(2,2,2-trichloroethoxy)carbonyl>-L-alanyl>-L-4-hydroxyproline ethyl ester(103654-87-1)
    11. EPA Substance Registry System: N--N'-<(2,2,2-trichloroethoxy)carbonyl>-L-alanyl>-L-4-hydroxyproline ethyl ester(103654-87-1)
  • 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: 103654-87-1(Hazardous Substances Data)

103654-87-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 103654-87-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,6,5 and 4 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 103654-87:
(8*1)+(7*0)+(6*3)+(5*6)+(4*5)+(3*4)+(2*8)+(1*7)=111
111 % 10 = 1
So 103654-87-1 is a valid CAS Registry Number.

103654-87-1Downstream Products

103654-87-1Relevant articles and documents

Angiotensin converting enzyme inhibitors. 10. Aryl sulfonamide substituted N-[1-carboxy-3-phenylpropyl]-L-alanyl-L-proline derivatives as novel antihypertensives

Mencel,Regan,Barton,Menard,Bruno,Calvo,Kornberg,Schwab,neiss,Suh

, p. 1606 - 1615 (2007/10/02)

Compounds 1a-g consisting of enalaprilat covalently bonded to aryl sulfonamides, including several known thiazide diuretics, were synthesized and tested for ACE inhibitory and diuretic and overall antihypertensive effects. All compounds were potent ACE in

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