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71436-70-9

1,3-Di-tert-butoxynaphthalin is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 71436-70-9 Structure

  • Basic information

    1. Product Name: 1,3-Di-tert-butoxynaphthalin
    2. Synonyms: 1,3-Di-tert-butoxynaphthalin
    3. CAS NO:71436-70-9
    4. Molecular Formula:
    5. Molecular Weight: 272.387
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 71436-70-9.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: 1,3-Di-tert-butoxynaphthalin(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,3-Di-tert-butoxynaphthalin(71436-70-9)
    11. EPA Substance Registry System: 1,3-Di-tert-butoxynaphthalin(71436-70-9)

  • 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: 71436-70-9(Hazardous Substances Data)

71436-70-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 71436-70-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,4,3 and 6 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 71436-70:
(7*7)+(6*1)+(5*4)+(4*3)+(3*6)+(2*7)+(1*0)=119
119 % 10 = 9
So 71436-70-9 is a valid CAS Registry Number.

71436-70-9Downstream Products

71436-70-9Relevant articles and documents

Generation of 2-Chloronaphthalene-1,3-diyl

Billups, W.E.,Buynak, John D.,Butler, Dorothy

, p. 4636 - 4641 (2007/10/02)

Reaction of 1-bromo-3,4-benzo-6,6-dichlorobicyclohexane with potassium tert-butoxide in tetrahydrofuran yields 2-chloronaphthalene along with nine other naphthalenes which result from solvent incorporation or reaction with nucleophile (Br-, Cl-, t-BuO-).Use of tetrahydrofuran-d8 as the solvent leads to the incorporation of two deuterium atoms into the chloronaphthalene.This result is interpreted in terms of a 1,3-dehydronaphthalene opening to the diradical, followed by abstraction of deuterium atoms from the solvent.The products which result from incorporation of solvent would then arise by dimerization of radical pairs.The remaining products are thought to arise from nucleophilic addition to the closed form of the dehydronaphthalene.

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