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CAS

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175439-85-7

4-bromobenzaldehyde trisylhydrazone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 175439-85-7 Structure

  • Basic information

    1. Product Name: 4-bromobenzaldehyde trisylhydrazone
    2. Synonyms: 4-bromobenzaldehyde trisylhydrazone
    3. CAS NO:175439-85-7
    4. Molecular Formula:
    5. Molecular Weight: 465.454
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 175439-85-7.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: 4-bromobenzaldehyde trisylhydrazone(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-bromobenzaldehyde trisylhydrazone(175439-85-7)
    11. EPA Substance Registry System: 4-bromobenzaldehyde trisylhydrazone(175439-85-7)

  • 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: 175439-85-7(Hazardous Substances Data)

175439-85-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 175439-85-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,5,4,3 and 9 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 175439-85:
(8*1)+(7*7)+(6*5)+(5*4)+(4*3)+(3*9)+(2*8)+(1*5)=167
167 % 10 = 7
So 175439-85-7 is a valid CAS Registry Number.

175439-85-7Relevant articles and documents

Alkylation of Aldehyde (Arenesulfonyl)hydrazones with Trialkylboranes

Kabalka, George W.,Maddox, John T.,Bogas, Ekaterini,Kelley, Shane W.

, p. 3688 - 3695 (2007/10/03)

(Arenesulfonyl)hydrazone derivatives of aryl aldehydes are readily alkylated by trialkylboranes in the presence of base to generate new organoboranes that may be converted to the corresponding substituted alkanes or alcohols depending upon the reaction conditions chosen. Both tosyl- and trisylhydrazone derivatives can be utilized in the reaction, which tolerates a variety of functional groups, making it a versatile alternative to both the Grignard and Suzuki-coupling reactions.

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