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C22H29IO2Si is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1207069-53-1 Structure
  • Basic information

    1. Product Name: C22H29IO2Si
    2. Synonyms: C22H29IO2Si
    3. CAS NO:1207069-53-1
    4. Molecular Formula:
    5. Molecular Weight: 480.461
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1207069-53-1.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: C22H29IO2Si(CAS DataBase Reference)
    10. NIST Chemistry Reference: C22H29IO2Si(1207069-53-1)
    11. EPA Substance Registry System: C22H29IO2Si(1207069-53-1)
  • 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: 1207069-53-1(Hazardous Substances Data)

1207069-53-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1207069-53-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,7,0,6 and 9 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1207069-53:
(9*1)+(8*2)+(7*0)+(6*7)+(5*0)+(4*6)+(3*9)+(2*5)+(1*3)=131
131 % 10 = 1
So 1207069-53-1 is a valid CAS Registry Number.

1207069-53-1Upstream product

1207069-53-1Downstream Products

1207069-53-1Relevant articles and documents

Total synthesis and biological assessment of (-)-Exiguolide and analogues

Fuwa, Haruhiko,Suzuki, Takaya,Kubo, Hiroshi,Yamori, Takao,Sasaki, Makoto

scheme or table, p. 2678 - 2688 (2011/04/15)

We describe herein an enantioselective total synthesis of (-)-exiguolide, the natural enantiomer. The methylene bis(tetrahydropyran) substructure was efficiently synthesized by exploiting olefin cross-metathesis for the assembly of readily available acycl

Total synthesis of (-)-exiguolide

Fuwa, Haruhiko,Sasaki, Makoto

supporting information; experimental part, p. 584 - 587 (2010/05/17)

[Chemical equation presented] Total synthesis of (-)-exiguolide, the natural enantiomer, has been accomplished for the first time. The bis(tetrahydropyran) subunit was efficiently synthesized via consecutive olefin cross-metathesis/intramolecular oxa-conj

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