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  • 1350623-73-2 Structure
  • Basic information

    1. Product Name: C36H56O7Si3
    2. Synonyms: C36H56O7Si3
    3. CAS NO:1350623-73-2
    4. Molecular Formula:
    5. Molecular Weight: 685.093
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1350623-73-2.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: C36H56O7Si3(CAS DataBase Reference)
    10. NIST Chemistry Reference: C36H56O7Si3(1350623-73-2)
    11. EPA Substance Registry System: C36H56O7Si3(1350623-73-2)
  • 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: 1350623-73-2(Hazardous Substances Data)

1350623-73-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1350623-73-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,0,6,2 and 3 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1350623-73:
(9*1)+(8*3)+(7*5)+(6*0)+(5*6)+(4*2)+(3*3)+(2*7)+(1*3)=132
132 % 10 = 2
So 1350623-73-2 is a valid CAS Registry Number.

1350623-73-2Relevant articles and documents

Stereocontrolled total synthesis of polygalolide A

Yamada, Hitomi,Adachi, Masaatsu,Isobe, Minoru,Nishikawa, Toshio

, p. 1428 - 1435 (2013/07/26)

The total synthesis of polygalolide A, a secondary metabolite that was isolated from a Chinese medicinal plant, is reported. A key issue in this synthesis was construction of an oxabicyclo[3.2.1] skeleton, which was solved by the development of an intramo

Total synthesis of polygalolide A

Adachi, Masaatsu,Yamada, Hitomi,Isobe, Minoru,Nishikawa, Toshio

, p. 6532 - 6535 (2012/02/15)

The total synthesis of polygalolide A was accomplished through intramolecular C-glycosylation of glucal modified with siloxyfuran. The siloxyfuran group and siloxy substituent at the C-3 position played crucial roles in allowing direct access to the highl

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