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1403229-22-0

1-(tert-butyl)-4-(3,7-dimethylocta-1,6-dien-3-yl)benzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1403229-22-0 Structure

  • Basic information

    1. Product Name: 1-(tert-butyl)-4-(3,7-dimethylocta-1,6-dien-3-yl)benzene
    2. Synonyms: 1-(tert-butyl)-4-(3,7-dimethylocta-1,6-dien-3-yl)benzene
    3. CAS NO:1403229-22-0
    4. Molecular Formula:
    5. Molecular Weight: 270.458
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1403229-22-0.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: 1-(tert-butyl)-4-(3,7-dimethylocta-1,6-dien-3-yl)benzene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(tert-butyl)-4-(3,7-dimethylocta-1,6-dien-3-yl)benzene(1403229-22-0)
    11. EPA Substance Registry System: 1-(tert-butyl)-4-(3,7-dimethylocta-1,6-dien-3-yl)benzene(1403229-22-0)

  • 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: 1403229-22-0(Hazardous Substances Data)

1403229-22-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1403229-22-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,0,3,2,2 and 9 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1403229-22:
(9*1)+(8*4)+(7*0)+(6*3)+(5*2)+(4*2)+(3*9)+(2*2)+(1*2)=110
110 % 10 = 0
So 1403229-22-0 is a valid CAS Registry Number.

1403229-22-0Downstream Products

1403229-22-0Relevant articles and documents

Ligand-controlled palladium-catalyzed regiodivergent suzuki-miyaura cross-coupling of allylboronates and aryl halides

Yang, Yang,Buchwald, Stephen L.

supporting information, p. 10642 - 10645 (2013/08/23)

An orthogonal set of catalyst systems has been developed for the Suzuki-Miyaura coupling of 3,3-disubstituted and 3-monosubstituted allylboronates with (hetero)aryl halides. These methods allow for the highly selective preparation of either the α- or the

Regioselective cross-coupling of allylboronic acid pinacol ester derivatives with aryl halides via Pd-PEPPSI-IPent

Farmer, Jennifer L.,Hunter, Howard N.,Organ, Michael G.

supporting information, p. 17470 - 17473 (2013/01/15)

The cross-coupling reactions of allylboronic acid pinacol ester derivatives with aryl and heteroaryl halides occurred with high selectivity (>97%) at the α-carbon of the allylboron reagent in the presence of Pd-PEPPSI-IPent precatalyst and 5 M KOH in refluxing THF. In the case of trisubstituted allylboronates with different substituents on the olefin, minor olefin geometry isomerization was observed (E/Z & 80/20).

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