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(3-Methyl-cyclobutyl)-methanol, with the molecular formula C6H12O, is a colorless liquid characterized by a slight sweet odor. It is a chemical compound that serves as a versatile solvent and intermediate in the synthesis of various chemicals and pharmaceuticals.

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  • 24070-81-3 Structure
  • Basic information

    1. Product Name: (3-Methyl-cyclobutyl)-methanol
    2. Synonyms: (3-Methyl-cyclobutyl)-methanol
    3. CAS NO:24070-81-3
    4. Molecular Formula: C6H12O
    5. Molecular Weight: 100.15888
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 24070-81-3.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 146.2°C at 760 mmHg
    3. Flash Point: 53.1°C
    4. Appearance: /
    5. Density: 0.914g/cm3
    6. Vapor Pressure: 1.85mmHg at 25°C
    7. Refractive Index: 1.449
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: (3-Methyl-cyclobutyl)-methanol(CAS DataBase Reference)
    11. NIST Chemistry Reference: (3-Methyl-cyclobutyl)-methanol(24070-81-3)
    12. EPA Substance Registry System: (3-Methyl-cyclobutyl)-methanol(24070-81-3)
  • 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: 24070-81-3(Hazardous Substances Data)

24070-81-3 Usage

Uses

Used in Paint and Coatings Industry:
(3-Methyl-cyclobutyl)-methanol is used as a solvent to facilitate the application and drying process of paints and coatings, enhancing their performance and durability.
Used in Adhesives Industry:
In the adhesives industry, (3-Methyl-cyclobutyl)-methanol is utilized as a solvent to improve the adhesive's bonding strength and workability.
Used in Chemical and Pharmaceutical Synthesis:
(3-Methyl-cyclobutyl)-methanol is used as an intermediate in the synthesis of other chemicals and pharmaceuticals, contributing to the development of new products and formulations.
Safety Precautions:
While (3-Methyl-cyclobutyl)-methanol is considered relatively low in toxicity, it is essential to handle and use it with proper safety measures. Prolonged exposure to high concentrations may cause irritation to the respiratory tract and skin.

Check Digit Verification of cas no

The CAS Registry Mumber 24070-81-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,0,7 and 0 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 24070-81:
(7*2)+(6*4)+(5*0)+(4*7)+(3*0)+(2*8)+(1*1)=83
83 % 10 = 3
So 24070-81-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H12O/c1-5-2-6(3-5)4-7/h5-7H,2-4H2,1H3

24070-81-3Relevant articles and documents

PYRIDINE-1-OXIDE DERIVATIVES AND THEIR USE AS FACTOR XIA INHIBITORS

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Page/Page column 45, (2018/03/25)

The present invention provides a compound of Formula (I) and pharmaceutical compositions comprising one or more said compounds, and methods for using said compounds for treating or preventing thromboses, embolisms, hypercoagulability or fibrotic changes. The compounds are selective Factor XIa inhibitors or dual inhibitors of Factor XIa and plasma kallikrein.

General Synthesis of Methyl- and Dimethyl-cyclobutanes from Simple 1,3-Diols by Phase Transfer Catalysis

Toeroek, Bela,Molnar, Arpad

, p. 801 - 804 (2007/10/02)

A general method is described for the preparation of methyl- and dimethyl-cyclobutanes from simple 1,3-diols.The key steps of the procedure are a phase transfer catalysed ring closure and the transformation of a carboxyl group to a methyl group.Phase transfer catalysis provides good yields in the synthesis of the cyclobutane skeleton.

Synthesis and Liquid Crystal Properties of Dimethylene Linked Compounds Incorporating the Cyclobutane or Spiroheptane Rings

Chan, L. K. M.,Gemmell, P. A.,Gray, G. W.,Lacey, D.,Toyne, K. J.

, p. 229 - 246 (2007/10/02)

The preparation of sixteen dimethylene linked compounds is described heptane ring>, and a comparison is made between the transition temperatures of these compounds and those of the corresponding esters.This comparison once again highlights the fact that the cyclobutane ring should be regarded, in terms of its ability to promote nematic thermal stability, as a "chain stiffener rather than as a ring system.A comparison is also made of the nematic thermal stabilities of the trans-cyclobutane and the spiroheptane systems and of the trans-cyclohexane and the spiroundecane systems.

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