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resorcin bis(tetrahydropyranyl)ether is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 30778-88-2 Structure
  • Basic information

    1. Product Name: resorcin bis(tetrahydropyranyl)ether
    2. Synonyms: resorcin bis(tetrahydropyranyl)ether
    3. CAS NO:30778-88-2
    4. Molecular Formula:
    5. Molecular Weight: 278.348
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 30778-88-2.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: resorcin bis(tetrahydropyranyl)ether(CAS DataBase Reference)
    10. NIST Chemistry Reference: resorcin bis(tetrahydropyranyl)ether(30778-88-2)
    11. EPA Substance Registry System: resorcin bis(tetrahydropyranyl)ether(30778-88-2)
  • 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: 30778-88-2(Hazardous Substances Data)

30778-88-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 30778-88-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,7,7 and 8 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 30778-88:
(7*3)+(6*0)+(5*7)+(4*7)+(3*8)+(2*8)+(1*8)=132
132 % 10 = 2
So 30778-88-2 is a valid CAS Registry Number.

30778-88-2Relevant articles and documents

N-Bromosuccinimide (NBS): A mild and efficient catalyst for tetrahydropyranylation of alcohols and phenols under solvent-free conditions

Khazaei, Ardeshir,Rostami, Amin,Raiatzadeh, Ayeh

, p. 1029 - 1032 (2007)

Different types of alcohols and phenols are tetrahydropyranylated in the presence of NBS catalyst in good to excellent yields under mild, neutral and solvent-free conditions.

Strategies for the synthesis of bi- and triarylic materials starting from commercially available phenols

Chopa, Alicia B.,Silbestri, Gustavo F.,Lockhart, María T.

, p. 3865 - 3877 (2007/10/03)

A series of arylstannanes have been synthesized, through an SRN1 mechanism, in good to excellent yields (74%-99%) by the photostimulated reaction of trimethyl stannyl ion with substrates supporting different nucleofugal groups. The arylstannanes thus obtained were suitable intermediates for Stille cross-coupling reactions leading to asymmetric bi- and triaryl compounds in acceptable global yields. An attractive feature of this route is that simple commercially available benzenediols, chloro- and methoxy phenols might be useful starting substrates, leading the latter to higher global yields of products in fewer steps. The strategies proposed open a broad synthetic tool.

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