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1449219-11-7

N-(hepta-1,6-dien-4-yl)-N-(4-methoxybenzyl)formamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1449219-11-7 Structure

  • Basic information

    1. Product Name: N-(hepta-1,6-dien-4-yl)-N-(4-methoxybenzyl)formamide
    2. Synonyms: N-(hepta-1,6-dien-4-yl)-N-(4-methoxybenzyl)formamide
    3. CAS NO:1449219-11-7
    4. Molecular Formula:
    5. Molecular Weight: 259.348
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1449219-11-7.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: N-(hepta-1,6-dien-4-yl)-N-(4-methoxybenzyl)formamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-(hepta-1,6-dien-4-yl)-N-(4-methoxybenzyl)formamide(1449219-11-7)
    11. EPA Substance Registry System: N-(hepta-1,6-dien-4-yl)-N-(4-methoxybenzyl)formamide(1449219-11-7)

  • 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: 1449219-11-7(Hazardous Substances Data)

1449219-11-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1449219-11-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,9,2,1 and 9 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1449219-11:
(9*1)+(8*4)+(7*4)+(6*9)+(5*2)+(4*1)+(3*9)+(2*1)+(1*1)=167
167 % 10 = 7
So 1449219-11-7 is a valid CAS Registry Number.

1449219-11-7Relevant articles and documents

Diaminophosphine oxide ligand enabled asymmetric nickel-catalyzed hydrocarbamoylations of alkenes

Donets, Pavel A.,Cramer, Nicolai

, p. 11772 - 11775 (2013/09/02)

Chiral trivalent phosphorus species are the dominant class of ligands and the key controlling element in asymmetric homogeneous transition-metal catalysis. Here, novel chiral diaminophosphine oxide ligands are described. The arising catalyst system with nickel(0) and trimethylaluminum efficiently activates formamide C-H bonds under mild conditions providing pyrrolidones via intramolecular hydrocarbamoylation in a highly enantioselective manner with as little as 0.25% mol catalyst loading. Mechanistically, the secondary phosphine oxides behave as bridging ligands for the nickel center and the Lewis acidic organoaluminum center to give a heterobimetallic catalyst with superior reactivity.

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