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56987-80-5

15,19-Dimethyltritriacontane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 56987-80-5 Structure

  • Basic information

    1. Product Name: 15,19-Dimethyltritriacontane
    2. Synonyms: 15,19-Dimethyltritriacontane
    3. CAS NO:56987-80-5
    4. Molecular Formula: C35H72
    5. Molecular Weight: 492.94618
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 56987-80-5.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 15,19-Dimethyltritriacontane(CAS DataBase Reference)
    10. NIST Chemistry Reference: 15,19-Dimethyltritriacontane(56987-80-5)
    11. EPA Substance Registry System: 15,19-Dimethyltritriacontane(56987-80-5)

  • 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: 56987-80-5(Hazardous Substances Data)

56987-80-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 56987-80-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,9,8 and 7 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 56987-80:
(7*5)+(6*6)+(5*9)+(4*8)+(3*7)+(2*8)+(1*0)=185
185 % 10 = 5
So 56987-80-5 is a valid CAS Registry Number.

56987-80-5Downstream Products

56987-80-5Relevant articles and documents

INSECT PHEROMONES AND THEIR ANALOGUES. XVIII. REGIOSPECIFIC SYNTHESIS OF (+/-)-15,19-DIMETHYLTRITRIACONTANE - A COMPONENT OF THE PHEROMONE OF Stomoxys calcitrans

Odinokov, V. N.,Akhmetova, V. R.,Savchenko, R. G.,Tolstikov, G. A.

, p. 500 - 502 (1987)

(+/-)-15,19-Dimethyltritriacontane (II) - a component of the pheromone of the stable fly - has been obtained by a five-stage synthesis from dimethylcyclooctadiene (I).The coupling of 1,1-dimethoxy-4-methyl-8-oxonon-4Z-ene with n-C13H27CH=PPh3 (THF; -30 deg C, 2 h; 25 deg C, 15 h; Ar) gave 1,1-dimethoxy-4,8-dimethyldocosa-4Z,8Z(E)-diene (III).The hydrolysis of (III) (TsOH.Py, H2O-Ac, boiling, 4 h) gave the corresponding aldehyde (IV).The condensation of (IV) with n-C10H21CH=PPh3 (THF; -60 to -30 deg C, 2 h, 25 deg C, 15 h) led to 15,19-dimethyltritriaconta-11Z(E),15Z,19Z(E)-triene (V), the exhaustive hydrogenation of which (ethanol, H2, 5percent Pd/C, 25 deg C) gave (II).The substance, the yield in percent, and Rf values are given, respectively: (II), 95, 0.92; (III), 29, 0.74; (IV), 80, 0.72; (V) 50, 0.8.The IR and PMR spectra of compounds (II)-(V) and the mass spectra of (II) and (III) are given.

INSECT PHEROMONES AND THEIR ANALOGUES XXIV. SYNTHESIS OF LONG-CHAIN 1,5-DIMETHYL-BRANCHED PHEROMONES FROM GERANYL ACETATE

Odinokov, V. N.,Ishmuratov, G. Yu.,Ladenkova, I. M.,Tolstikov, G. A.

, p. 697 - 701 (2007/10/02)

Schemes for the synthesis of long-chain 1,5-dimethyl-branched pheromones (7,11-dimethyloctadecane, 15,19-dimethyltritriacontane, and 2-acetoxy-3,7-dimethylpentadecane) from the product of allyl oxidation of geranyl acetate (8-acetoxy-2,6-dimethylocta-2E,6E-dien-1-ol) have been developed.

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