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1290043-08-1

3-((tert-butyldiphenylsilyl)oxy)-2-chloropropanal is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1290043-08-1 Structure

  • Basic information

    1. Product Name: 3-((tert-butyldiphenylsilyl)oxy)-2-chloropropanal
    2. Synonyms: 3-((tert-butyldiphenylsilyl)oxy)-2-chloropropanal
    3. CAS NO:1290043-08-1
    4. Molecular Formula:
    5. Molecular Weight: 346.929
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1290043-08-1.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: 3-((tert-butyldiphenylsilyl)oxy)-2-chloropropanal(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-((tert-butyldiphenylsilyl)oxy)-2-chloropropanal(1290043-08-1)
    11. EPA Substance Registry System: 3-((tert-butyldiphenylsilyl)oxy)-2-chloropropanal(1290043-08-1)

  • 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: 1290043-08-1(Hazardous Substances Data)

1290043-08-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1290043-08-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,9,0,0,4 and 3 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1290043-08:
(9*1)+(8*2)+(7*9)+(6*0)+(5*0)+(4*4)+(3*3)+(2*0)+(1*8)=121
121 % 10 = 1
So 1290043-08-1 is a valid CAS Registry Number.

1290043-08-1Downstream Products

1290043-08-1Relevant articles and documents

Synthesis of chiral N-sulfonyl and N-phosphinoyl α-halo aldimine precursors

Stanton, Gretchen R.,Goellue, Mehmet,Platoff, Rebecca M.,Rich, Corinne E.,Carroll, Patrick J.,Walsh, Patrick J.

, p. 757 - 764 (2013)

α-Halogenated aldimines have emerged as an important class of synthetic intermediates. The stability and reactivity of α-halo aldimines can vary greatly depending on the nitrogen protecting group. A general synthesis of stable, chiral α-halo-N-sulfonyl an

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