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C59H95Cl3O16Si2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 218799-03-2 Structure
  • Basic information

    1. Product Name: C59H95Cl3O16Si2
    2. Synonyms: C59H95Cl3O16Si2
    3. CAS NO:218799-03-2
    4. Molecular Formula:
    5. Molecular Weight: 1222.92
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 218799-03-2.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: C59H95Cl3O16Si2(CAS DataBase Reference)
    10. NIST Chemistry Reference: C59H95Cl3O16Si2(218799-03-2)
    11. EPA Substance Registry System: C59H95Cl3O16Si2(218799-03-2)
  • 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: 218799-03-2(Hazardous Substances Data)

218799-03-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 218799-03-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,8,7,9 and 9 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 218799-03:
(8*2)+(7*1)+(6*8)+(5*7)+(4*9)+(3*9)+(2*0)+(1*3)=172
172 % 10 = 2
So 218799-03-2 is a valid CAS Registry Number.

218799-03-2Upstream product

218799-03-2Downstream Products

218799-03-2Relevant articles and documents

Studies in marine macrolide synthesis: Synthesis of a fully functionalised C1-C28 subunit of spongistatin 1 (Altohyrtin A)

Paterson, Ian,Wallace, Debra J.,Oballa, Renata M.

, p. 8545 - 8548 (1998)

The C1-C28 aldehyde 5, containing the AB- and CD-spiroacetal portions together with the bridging chain of spongistatin 1 (1), was prepared. The key step was a lithium-mediated, anti-aldol coupling between ethyl ketone 4 and aldehyde

The stereocontrolled total synthesis of altohyrtin A/spongistatin 1: Fragment couplings, completion of the synthesis, analogue generation and biological evaluation

Paterson, Ian,Chen, David Y.-K.,Coster, Mark J.,Acena, Jose L.,Bach, Jordi,Wallace, Debra J.

, p. 2431 - 2440 (2007/10/03)

The antimitotic marine macrolide altohyrtin A/spongistatin 1 (1) has been synthesised in a highly convergent and stereocontrolled manner, thus contributing to the replenishment of the largely exhausted material from the initial isolation work. Coupling of

Stereocontrolled total synthesis of (+)-altohyrtin A/spongistatin 1

Paterson, Ian,Chen, David Y.-K.,Coster, Mark J.,Acea, Jose L.,Bach, Jordi,Gibson, Karl R.,Keown, Linda E.,Oballa, Renata M.,Trieselmann, Thomas,Wallace, Debra J.

, p. 4055 - 4060 (2007/10/03)

As an exceptionally potent antimitotic macrolide, altohyrtin A/spongistatin 1 shows great promise in cancer chemotherapy but its extreme scarcity in the natural sponges has halted its further preclinical development. A highly stereocontrolled total synthe

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