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CAS

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92344-81-5

endo-3-Tetracyclo<5.3.1.02,6.04,9>undecanemethanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 92344-81-5 Structure

  • Basic information

    1. Product Name: endo-3-Tetracyclo<5.3.1.02,6.04,9>undecanemethanol
    2. Synonyms:
    3. CAS NO:92344-81-5
    4. Molecular Formula:
    5. Molecular Weight: 178.274
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 92344-81-5.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: endo-3-Tetracyclo<5.3.1.02,6.04,9>undecanemethanol(CAS DataBase Reference)
    10. NIST Chemistry Reference: endo-3-Tetracyclo<5.3.1.02,6.04,9>undecanemethanol(92344-81-5)
    11. EPA Substance Registry System: endo-3-Tetracyclo<5.3.1.02,6.04,9>undecanemethanol(92344-81-5)

  • 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: 92344-81-5(Hazardous Substances Data)

92344-81-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 92344-81-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,3,4 and 4 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 92344-81:
(7*9)+(6*2)+(5*3)+(4*4)+(3*4)+(2*8)+(1*1)=135
135 % 10 = 5
So 92344-81-5 is a valid CAS Registry Number.

92344-81-5Upstream product

92344-81-5Downstream Products

92344-81-5Relevant articles and documents

Reaction of 3,5-Dehydronoriceane with Tetracarbonylbis(μ-chloro)dirhodium : Evidence for the Oxidative Addition of Rh(I) Complex to a Bicyclopentane System

Yamaguchi, Ryohei,Kawanisi, Mituyosi

, p. 4460 - 4462 (1984)

A stoichiometric reaction of the title compound (1) with Rh2(CO)4Cl2 gives a stable acylrhodium complex (3).This is the first experimental evidence for the oxidative addition of Rh(I) complex to a bicyclopentane system.Treatment of 3 with 2 equiv of triphenylphosphine gives rise to the starting bicyclopentane (1), instead of a keto compound.This contrasts markedly with reactions of acylrhodium complexes derived from other strained systems with triphenylphosphine to yield ketones.The structure of 3 is further confirmed by hydride reduction of 3 affording exo-3-(hydroxymethyl)noriceane (8), along with a small amount of two hydrocarbons, noriceane (9) and exo-3-methylnoriceane (10).

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