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  • 1198597-04-4 Structure
  • Basic information

    1. Product Name: C30H42N2O6
    2. Synonyms: C30H42N2O6
    3. CAS NO:1198597-04-4
    4. Molecular Formula:
    5. Molecular Weight: 526.673
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1198597-04-4.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: C30H42N2O6(CAS DataBase Reference)
    10. NIST Chemistry Reference: C30H42N2O6(1198597-04-4)
    11. EPA Substance Registry System: C30H42N2O6(1198597-04-4)
  • 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: 1198597-04-4(Hazardous Substances Data)

1198597-04-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1198597-04-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,8,5,9 and 7 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1198597-04:
(9*1)+(8*1)+(7*9)+(6*8)+(5*5)+(4*9)+(3*7)+(2*0)+(1*4)=214
214 % 10 = 4
So 1198597-04-4 is a valid CAS Registry Number.

1198597-04-4Relevant articles and documents

Monotelechelic poly(oxa)norbornenes by ring-opening metathesis polymerization using direct end-capping and cross-metathesis

Matson, John B.,Grubbs, Robert H.

, p. 213 - 221 (2010)

Two different methodologies for the synthesis of monotelechelic poly(oxa)norbornenes prepared by living ring-opening metathesis polymerization (ROMP) are presented. The first method, termed direct end-capping, is carried out by adding an internal ciss-olefin terminating agent (TA) to the reaction mixture immediately after the completion of the living ROMP reaction. The second method relies on crossmetathesis (CM) between a methylene-terminated poly(oxa)norbornene and a cis-olefin TA mediated by the ruthenium olefin metathesis catalyst (H2IMeS)(Cl)2Ru(CH-o-OiPrC 6H4) (H2IMeS = 1,3-dimesitylimidazolidine-2- ylidene). TAs containing various functional groups, including alcohols, acetates, bromides, a-bromoesters, thioacetates, N-hydroxysuccinimidyl esters, and Boc-amines, as well as fluorescein and biotin groups, were synthesized and tested. The direct end-capping method typically resulted in > 90% endfunctionalization efficiency, while the CM method was nearly as effective for TAs without polar functional groups or significant steric bulk. End-functionalization efficiency values were determined by 1H NMR spectroscopy.

Synthesis of hybrid block copolymers via integrated ring-opening metathesis polymerization and polymerization of NCA

Bai, Yugang,Lu, Hua,Ponnusamy, Ettigounder,Cheng, Jianjun

supporting information; experimental part, p. 10830 - 10832 (2011/11/04)

Linear hybrid block copolymers with well controlled molecular weights and narrow polydispersities were synthesized via ring-opening metathesis polymerization (ROMP) followed by ring-opening polymerization of amino acid N-carboxyanhydrides.

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