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804556-39-6

Heptanenitrile, 2-hydroxy-7-(triphenylmethoxy)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 804556-39-6 Structure

  • Basic information

    1. Product Name: Heptanenitrile, 2-hydroxy-7-(triphenylmethoxy)-
    2. Synonyms:
    3. CAS NO:804556-39-6
    4. Molecular Formula: C26H27NO2
    5. Molecular Weight: 385.506
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 804556-39-6.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: Heptanenitrile, 2-hydroxy-7-(triphenylmethoxy)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Heptanenitrile, 2-hydroxy-7-(triphenylmethoxy)-(804556-39-6)
    11. EPA Substance Registry System: Heptanenitrile, 2-hydroxy-7-(triphenylmethoxy)-(804556-39-6)

  • 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: 804556-39-6(Hazardous Substances Data)

804556-39-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 804556-39-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,0,4,5,5 and 6 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 804556-39:
(8*8)+(7*0)+(6*4)+(5*5)+(4*5)+(3*6)+(2*3)+(1*9)=166
166 % 10 = 6
So 804556-39-6 is a valid CAS Registry Number.

804556-39-6Downstream Products

804556-39-6Relevant articles and documents

Enzymatic acylation reactions on ω-hydroxycyanohydrins

Gonzalo, Gonzalo De,Lavandera, Iván,Brieva, Rosario,Gotor, Vicente

, p. 10525 - 10532 (2007/10/03)

The enzymatic acylation of certain ω-hydroxycyanohydrins protected at the primary alcohol has been studied. The best enantioselectivities are obtained with Pseudomonas cepacia lipase (PSL-C) and Candida antarctica lipase A (CAL-A), for the ω-O-tritylated cyanohydrins. The effect of the protecting group in the enzymatic reactions has been studied using molecular modeling. Graphical abstract.

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