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359844-32-9

2-allyl-6-chloro-4-methoxy-phenol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 359844-32-9 Structure

  • Basic information

    1. Product Name: 2-allyl-6-chloro-4-methoxy-phenol
    2. Synonyms:
    3. CAS NO:359844-32-9
    4. Molecular Formula:
    5. Molecular Weight: 198.649
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 359844-32-9.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: 2-allyl-6-chloro-4-methoxy-phenol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-allyl-6-chloro-4-methoxy-phenol(359844-32-9)
    11. EPA Substance Registry System: 2-allyl-6-chloro-4-methoxy-phenol(359844-32-9)

  • 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: 359844-32-9(Hazardous Substances Data)

359844-32-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 359844-32-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,9,8,4 and 4 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 359844-32:
(8*3)+(7*5)+(6*9)+(5*8)+(4*4)+(3*4)+(2*3)+(1*2)=189
189 % 10 = 9
So 359844-32-9 is a valid CAS Registry Number.

359844-32-9Upstream product

359844-32-9Relevant articles and documents

A biomimetic approach to dihydrobenzofuran synthesis

Benbow,Katoch-Rouse

, p. 4965 - 4972 (2001)

A method for an acid-catalyzed construction of dihydrobenzofuran heterocycles (14) from 2-(2′-hydroxyethyl)quinone precursors 10 is presented. The putative oxonium ion intermediate 17 formed by an intramolecular hydroxyl cyclization followed by dehydration is reduced in situ by an added dihydroquinone source. Good to excellent yields of cyclized products are realized in all cases except for highly electron deficient systems, and these suffer reduction prior to oxonium ion formation. All products are monomeric and derived from a two-electron transfer except for 10g, which affords the dimeric dihydrobenzofuran. The amount of cyclization or reduction product is governed by the HOMO/LUMO gap between the quinone substrate and the dihydroquinone additive, and the product distribution can be adjusted by modifying the electronic properties of the added reducing agent.

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