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1445875-26-2

C18H30O3Si is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1445875-26-2 Structure

  • Basic information

    1. Product Name: C18H30O3Si
    2. Synonyms: C18H30O3Si
    3. CAS NO:1445875-26-2
    4. Molecular Formula:
    5. Molecular Weight: 322.52
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1445875-26-2.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: C18H30O3Si(CAS DataBase Reference)
    10. NIST Chemistry Reference: C18H30O3Si(1445875-26-2)
    11. EPA Substance Registry System: C18H30O3Si(1445875-26-2)

  • 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: 1445875-26-2(Hazardous Substances Data)

1445875-26-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1445875-26-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,5,8,7 and 5 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1445875-26:
(9*1)+(8*4)+(7*4)+(6*5)+(5*8)+(4*7)+(3*5)+(2*2)+(1*6)=192
192 % 10 = 2
So 1445875-26-2 is a valid CAS Registry Number.

1445875-26-2Relevant articles and documents

Taming of a superbase for selective phenol desilylation and natural product isolation

Trader, Darci J.,Carlson, Erin E.

, p. 7349 - 7355 (2013/08/23)

Hydroxyl moieties are highly prevalent in natural products. We previously reported a chemoselective strategy for enrichment of hydroxyl-functionalized molecules by formation of a silyl ether bond to a resin. To generate smaller pools of molecules for analysis, we developed cleavage conditions to promote stepwise release of phenolic silyl ethers followed by aliphatic silyl ethers with a "tamed" version of the superbase 1,1,3,3-tetramethylguanadine. We demonstrate this as a general strategy for selective deprotection of phenolic silyl ethers under neutral conditions at room temperature.

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