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diethyl 10-undecenylmalonate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 52355-51-8 Structure
  • Basic information

    1. Product Name: diethyl 10-undecenylmalonate
    2. Synonyms: diethyl 10-undecenylmalonate
    3. CAS NO:52355-51-8
    4. Molecular Formula:
    5. Molecular Weight: 312.45
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 52355-51-8.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: diethyl 10-undecenylmalonate(CAS DataBase Reference)
    10. NIST Chemistry Reference: diethyl 10-undecenylmalonate(52355-51-8)
    11. EPA Substance Registry System: diethyl 10-undecenylmalonate(52355-51-8)
  • 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: 52355-51-8(Hazardous Substances Data)

52355-51-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 52355-51-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,3,5 and 5 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 52355-51:
(7*5)+(6*2)+(5*3)+(4*5)+(3*5)+(2*5)+(1*1)=108
108 % 10 = 8
So 52355-51-8 is a valid CAS Registry Number.

52355-51-8Relevant articles and documents

Total Synthesis of Laucysteinamide A, a Monomeric Congener of Somocystinamide A

Taylor, Kimberly S.,Zhang, Chen,Glukhov, Evgenia,Gerwick, William H.,Suyama, Takashi L.

, p. 865 - 870 (2021)

Laucysteinamide A (4) is a marine natural product isolated from the cyanobacterium Caldora penicillata and contains structural motifs found in promising cancer drug leads. The first total synthesis of 4 and its analogues was achieved, which also enabled a concise formal synthesis of somocystinamide A (3), a dimeric congener of 4 that previously showed extremely potent antiproliferative activities. This work provides further insights on structure-activity relationships in this class of natural products.

AVOIDANCE OF NON-SPECIFIC BINDING ON AN ACOUSTIC WAVE BIOSENSOR USING LINKER AND DILUENT MOLECULES FOR DEVICE SURFACE MODIFICATION

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Page/Page column 5, (2012/01/03)

An acoustic wave biosensor comprising a surface of a mixed self-assembling monolayer for receiving a probe-biomolecule is described herein. The biosensor surface may comprise a piezoelectric quartz crystal,—for detection purposes with the electromagnetic piezoelectric acoustic sensor (EMPAS)—upon which a mixed self-assembling monolayer is formed, which includes at least one linker, such as 2,2,2-trifluoroethyl-13-trichlorosilyl-tridecanoate (TTTA); its oligoethylene glycol (OEG) analog OEGylated TTTA (OEG-TTTA); S-(2-(2-(2-(3-trichlorosilyl-propyloxy)-ethoxy)-ethoxy)-ethyl)-benzenethiosulfonate (OEG-TU BTS). Linker/diluent systems for attaching a functionalizing entity to the surface of a biosensor are described, as well as methods for preparing a biosensor surface with an oligoethylene glycol linker.

Polyanion inhibitors of human immunodeficiency virus. Part IV. - Polymerized anionic surfactants : Influence of the density and distribution of anionic groups on the antiviral activity

Leydet, Alain,Barthelemy, Philippe,Boyer, Bernard,Lamaty, Gerard,Roque, Jean-Pierre,Witvrouw, Myriam,De Clercq, Erik

, p. 397 - 402 (2007/10/03)

The synthesis of a series of new polyanions, via γ-polymerization, of ω-unsaturated multi-charged anionic surfactants, has been realized. These polyanions were evaluated for their activity against HIV-1. All tested compounds proved active without presenting toxicity to the host cells (CEM-4 or MT-4).

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