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122211-09-0

C29H26O is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 122211-09-0 Structure

  • Basic information

    1. Product Name: C29H26O
    2. Synonyms:
    3. CAS NO:122211-09-0
    4. Molecular Formula:
    5. Molecular Weight: 390.525
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 122211-09-0.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: C29H26O(CAS DataBase Reference)
    10. NIST Chemistry Reference: C29H26O(122211-09-0)
    11. EPA Substance Registry System: C29H26O(122211-09-0)

  • 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: 122211-09-0(Hazardous Substances Data)

122211-09-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 122211-09-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,2,2,1 and 1 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 122211-09:
(8*1)+(7*2)+(6*2)+(5*2)+(4*1)+(3*1)+(2*0)+(1*9)=60
60 % 10 = 0
So 122211-09-0 is a valid CAS Registry Number.

122211-09-0Downstream Products

122211-09-0Relevant articles and documents

Synthesis of a Highly Strained Cyclopropene: Tricyclo2,4>non-2(4)-ene

Chenier, Philip J.,Southars, Dale A.

, p. 3519 - 3520 (1989)

Tricyclo2,4>non-2(4)-ene has been synthesized.This is one of the most highly strained cyclopropenes yet reported.It can be made by treatment of a vicinal dibromocyclopropane with tert-butyllithium in THF at -78 deg C.It was identified b

Tricyclo2,4>non-2(4)-ene: Synthesis and Trapping of a Strained Cyclopropene

Chenier, Philip J.,Southard, Dale A.

, p. 4333 - 4337 (2007/10/02)

The title compound 8 has been synthesized in situ from dibromide 18 via debromination with tert.-butyllithium in THF at -78 deg C.In the presence of diphenylisobenzofuran (27), the Diels-Alder adduct 29 is formed.Cyclopropene 8 was also trapped with diene 28 to give a second adduct 30.The synthetic methodology for precursor dibromide 18 appears to have general application for other similar highly strained tricyclic cyclopropenes.

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