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186743-34-0

3-methylallylguaiacol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 186743-34-0 Structure

  • Basic information

    1. Product Name: 3-methylallylguaiacol
    2. Synonyms: 3-methylallylguaiacol
    3. CAS NO:186743-34-0
    4. Molecular Formula:
    5. Molecular Weight: 178.231
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 186743-34-0.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: 3-methylallylguaiacol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-methylallylguaiacol(186743-34-0)
    11. EPA Substance Registry System: 3-methylallylguaiacol(186743-34-0)

  • 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: 186743-34-0(Hazardous Substances Data)

186743-34-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 186743-34-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,6,7,4 and 3 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 186743-34:
(8*1)+(7*8)+(6*6)+(5*7)+(4*4)+(3*3)+(2*3)+(1*4)=170
170 % 10 = 0
So 186743-34-0 is a valid CAS Registry Number.

186743-34-0Relevant articles and documents

Towards the total synthesis of neurotrophically active tashironins: rapid construction of the tetracyclic core through a tandem oxidative dearomatization-IMDA reaction-RCM protocol

Mehta, Goverdhan,Maity, Pulakesh

, p. 8865 - 8868 (2008/03/30)

An exceptionally short (three step) strategy involving tandem oxidative dearomatization, intramolecular Diels-Alder (IMDA) reaction and RCM has been devised to generate the complete carbon framework present in tashironin-type sesquiterpenoid natural produ

Skin sensitization to eugenol and isoeugenol in mice: Possible metabolic pathways involving ortho-quinone and quinone methide intermediates

Bertrand, Franck,Basketter, David A.,Roberts, David W.,Lepoittevin, Jean-Pierre

, p. 335 - 343 (2007/10/03)

With the aim of providing further mechanistic insights into the mode of action of eugenol (4-allyl-2-methoxyphenol) and isoeugenol (4-propenyl-2- methoxyphenol), we have synthesized two series of modified compounds which were tested in the mouse local lym

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