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95712-44-0

N-benzyl-N-<1-methoxymethyloxypent-2(Z)-en-5-yl>crotonamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 95712-44-0 Structure

  • Basic information

    1. Product Name: N-benzyl-N-<1-methoxymethyloxypent-2(Z)-en-5-yl>crotonamide
    2. Synonyms: N-benzyl-N-<1-methoxymethyloxypent-2(Z)-en-5-yl>crotonamide
    3. CAS NO:95712-44-0
    4. Molecular Formula:
    5. Molecular Weight: 303.401
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 95712-44-0.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: N-benzyl-N-<1-methoxymethyloxypent-2(Z)-en-5-yl>crotonamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-benzyl-N-<1-methoxymethyloxypent-2(Z)-en-5-yl>crotonamide(95712-44-0)
    11. EPA Substance Registry System: N-benzyl-N-<1-methoxymethyloxypent-2(Z)-en-5-yl>crotonamide(95712-44-0)

  • 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: 95712-44-0(Hazardous Substances Data)

95712-44-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 95712-44-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,7,1 and 2 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 95712-44:
(7*9)+(6*5)+(5*7)+(4*1)+(3*2)+(2*4)+(1*4)=150
150 % 10 = 0
So 95712-44-0 is a valid CAS Registry Number.

95712-44-0Relevant articles and documents

APPLICATION OF THE INTRAMOLECULAR DIELS-ALDER REACTIONS OF HETERODIENES TO THE SYNTHESES OF INDOLE ALKALOIDS

Martin, Stephen F.,Benage, Brigitte,Williamson, Sidney A.,Brown, Stephen P.

, p. 2903 - 2910 (2007/10/02)

A novel intramolecular Diels-Alder reaction involving the addition of an α,β-unsaturated aldehyde to an electron-deficient, dienophilic partner has been exploited as the key step in the development of a general entry to the heteroyohimboid and corynanthei

APPLICATIONS OF INTRAMOLECULAR DIELS-ALDER REACTIONS OF HETERODIENES. FACILE SYNTHESES OF HETEROYOHIMBINE ALKALOIDS TETRAHYDROALSTONINE AND AKUAMMIGINE

Martin, Stephen F.,Benage, Brigitte

, p. 4863 - 4866 (2007/10/02)

A facile, formal synthesis of the heteroyohimbine alkaloids tetrahydroalstonine (1) and akuammigine (2) has been completed in which the D/E ring system is constructed by the novel cyclization of the triene 10, a process which involves the intramolecular

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