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  • 1356446-78-0 Structure
  • Basic information

    1. Product Name: Fosinopril impurity D
    2. Synonyms: Fosinopril impurity D;(4R)-4-Cyclohexyl-1-[(R)-[(S)-1-hydroxy-2-Methylpropoxy](4-phenylbutyl)phosphinyl]acetyl-L-proline Propionate SodiuM Salt;(2S,4R)-4-Cyclohexyl-1-[[(R)-[(1S)-2-methyl-1-(1-oxopropoxy)propoxy](4-phenylbutyl)phosphoryl]acetyl]pyrrolidine-2-carboxylic acid
    3. CAS NO:1356446-78-0
    4. Molecular Formula: C30H46NO7P
    5. Molecular Weight: 563.66
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1356446-78-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Fosinopril impurity D(CAS DataBase Reference)
    10. NIST Chemistry Reference: Fosinopril impurity D(1356446-78-0)
    11. EPA Substance Registry System: Fosinopril impurity D(1356446-78-0)
  • 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: 1356446-78-0(Hazardous Substances Data)

1356446-78-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1356446-78-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,6,4,4 and 6 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1356446-78:
(9*1)+(8*3)+(7*5)+(6*6)+(5*4)+(4*4)+(3*6)+(2*7)+(1*8)=180
180 % 10 = 0
So 1356446-78-0 is a valid CAS Registry Number.

1356446-78-0 Well-known Company Product Price

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  • Sigma-Aldrich

  • (Y0001231)  Fosinopril impurity D  European Pharmacopoeia (EP) Reference Standard

  • 1356446-78-0

  • Y0001231

  • 1,880.19CNY

  • Detail

1356446-78-0Downstream Products

1356446-78-0Relevant articles and documents

Preparation methods of antihypertensive Fosinopril sodium and key intermediate thereof

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, (2017/12/14)

The invention relates to preparation methods of an antihypertensive Fosinopril sodium and a key intermediate thereof trans-4-phenyl-L-proline suitable for industrial production. Synthesis of the key intermediate trans-4-phenyl-L-proline has high chiral selectivity, and the method is simple and easy to operate.

COMPOSITIONS AND METHODS FOR DIAGNOSING AND TREATING SALT SENSITIVITY OF BLOOD PRESSURE

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, (2015/02/05)

To characterize the urinary exosome miRNome, microarrays were used to identify the miRNA spectrum present within urinary exosomes from ten individuals that were previously classified for their salt sensitivity status. The present application discloses distinct patterns of selected exosomal miRNA expression that were different between salt-sensitive (SS), salt-resistant (SR), and inverse salt-sensitive (ISS) individuals. These miRNAs can be useful as biomarkers either individually or as panels comprising multiple miRNAs. The present invention provides compositions and methods for identifying, diagnosing, monitoring, and treating subjects with salt sensitivity of blood pressure. The applications discloses panels of miRNAs useful for comparing profiles, and in some cases one or more of the miRNAs in a panel can be used. The miRNAs useful for distinguishing SS and SR or ISS and SR subjects. One or more of the 45 miRNAs can be used. Some of the miRNAs have not been previously reported to be circulating. See those miRNAs with asterisks in FIG. 1 and below. The present invention encompasses the use of one or more of these markers for identifying and diagnosing SR, SS, and ISS subjects.

Process for the preparation of fosinopril and intermediates thereof

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Page/Page column 7, (2012/06/18)

The present invention relates to a process for the preparation of intermediates useful in the synthesis of [1[S(R)],2α,4β]-4-cyclohexyl-1-[[[2-methyl-1-oxypropoxy) propoxy](4-phenylbutyl phosphinyl]acetyl]-L-proline, and the synthesis thereof, in particular as sodium salt (fosinopril sodium).

PROCESS FOR THE PREPARATION OF FOSINOPRIL AND INTERMEDIATES THEREOF

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Page/Page column 5, (2012/06/16)

The present invention relates to a process for the preparation of intermediates useful in the synthesis of [1[S(R)],2α,4β]-4-cyclohexyl-1-[[[2-methyl-1-oxypropoxy)propoxy](4-phenylbutyl phosphinyl]acetyl]L-proline, and the synthesis thereof, in particular as sodium salt (fosinopril sodium).

Process for the preparation of fosinopril and intermediates thereof

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Page/Page column 7, (2011/01/11)

Process for the preparation of intermediates useful in the synthesis of [1[S(R)],2α,4β]-4-cyclohexyl-1-[[[(2-methyl-1-oxypropoxy) propoxy](4-phenylbutyl) phosphinyl]acetyl]-L-proline, and the synthesis thereof, in particular as sodium salt.

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