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1018449-53-0

3',4'-bis(tert-butyldimethylsiloxy)-3,5-dihydroxystilbene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1018449-53-0 Structure

  • Basic information

    1. Product Name: 3',4'-bis(tert-butyldimethylsiloxy)-3,5-dihydroxystilbene
    2. Synonyms: 3',4'-bis(tert-butyldimethylsiloxy)-3,5-dihydroxystilbene
    3. CAS NO:1018449-53-0
    4. Molecular Formula:
    5. Molecular Weight: 472.772
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1018449-53-0.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: 3',4'-bis(tert-butyldimethylsiloxy)-3,5-dihydroxystilbene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3',4'-bis(tert-butyldimethylsiloxy)-3,5-dihydroxystilbene(1018449-53-0)
    11. EPA Substance Registry System: 3',4'-bis(tert-butyldimethylsiloxy)-3,5-dihydroxystilbene(1018449-53-0)

  • 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: 1018449-53-0(Hazardous Substances Data)

1018449-53-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1018449-53-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,1,8,4,4 and 9 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1018449-53:
(9*1)+(8*0)+(7*1)+(6*8)+(5*4)+(4*4)+(3*9)+(2*5)+(1*3)=140
140 % 10 = 0
So 1018449-53-0 is a valid CAS Registry Number.

1018449-53-0Downstream Products

1018449-53-0Relevant articles and documents

Biomimetic preparation of the racemic modifications of the stilbenolignan aiphanol and three congeners

Chand, Satish,Banwell, Martin G.

, p. 243 - 250 (2008/02/11)

A chromatographically separable mixture of the racemic modification, (±)-1, of the stilbenolignan (-)-aiphanol and congeners (±)-2-4 has been generated by a silver(I)-mediated and potentially biomimetic oxidative coupling of piceatannol (5) with sinapic a

Convergent synthesis and preliminary biological evaluations of the stilbenolignan (+/-)-aiphanol and various congeners.

Banwell, Martin G,Bezos, Anna,Chand, Satish,Dannhardt, Gerd,Kiefer, Werner,Nowe, Ulrike,Parish, Christopher R,Savage, G Paul,Ulbrich, Holger

, p. 2427 - 2429 (2007/10/03)

Treatment of an equimolar mixture of stilbene 7 and cinnamyl alcohol 8 with silver carbonate in acetone-benzene afforded a ca. 2:1:2:1 mixture of the stilbenolignan (+/-)-aiphanol (1) and congeners 2-4 each of which show significant anti-angiogenic and CO

SYNTHESIS OF NATURAL POLYHYDROXYSTILBENES

Cardona, Luz,Fernandez, Isabel,Garcia, Begona,Pedro, Jose R.

, p. 2725 - 2730 (2007/10/02)

A synthesis of several natural polyhydroxystilbenes is described.

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