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(3-allyloxetan-3-yl)methanol is a chemical compound with the molecular formula C7H12O2. It is a type of alcohol that contains an allyl group and an oxetane ring. This unique structure and reactivity make it a versatile compound with diverse potential uses in the field of chemistry and material science.

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  • 135939-47-8 Structure
  • Basic information

    1. Product Name: (3-allyloxetan-3-yl)methanol
    2. Synonyms: (3-allyloxetan-3-yl)methanol
    3. CAS NO:135939-47-8
    4. Molecular Formula: C7H12O2
    5. Molecular Weight: 128
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 135939-47-8.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: (3-allyloxetan-3-yl)methanol(CAS DataBase Reference)
    10. NIST Chemistry Reference: (3-allyloxetan-3-yl)methanol(135939-47-8)
    11. EPA Substance Registry System: (3-allyloxetan-3-yl)methanol(135939-47-8)
  • 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: 135939-47-8(Hazardous Substances Data)

135939-47-8 Usage

Uses

Used in Organic Synthesis:
(3-allyloxetan-3-yl)methanol is used as a building block in organic synthesis for its ability to contribute to the formation of various complex organic molecules.
Used in Pharmaceutical Production:
(3-allyloxetan-3-yl)methanol is used as an intermediate in the production of pharmaceuticals due to its potential to be incorporated into the structures of new drugs.
Used in Agrochemical Production:
(3-allyloxetan-3-yl)methanol is used as a component in the synthesis of agrochemicals, contributing to the development of new pesticides or other agricultural products.
Used in Fine Chemicals Production:
(3-allyloxetan-3-yl)methanol is used as a precursor in the production of fine chemicals, which are high-purity chemicals used in various industries.
Used in Polymer Synthesis:
(3-allyloxetan-3-yl)methanol is used as a monomer or a component in the synthesis of polymers, which can be utilized in a wide range of applications from plastics to coatings.
Used as a Reagent in Chemical Reactions:
(3-allyloxetan-3-yl)methanol is used as a reagent in various chemical reactions, facilitating specific transformations or processes in the synthesis of other compounds.
Used in Material Science:
(3-allyloxetan-3-yl)methanol has potential applications in the development of new materials due to its unique structure and reactivity, which can contribute to the creation of innovative materials with specific properties.

Check Digit Verification of cas no

The CAS Registry Mumber 135939-47-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,9,3 and 9 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 135939-47:
(8*1)+(7*3)+(6*5)+(5*9)+(4*3)+(3*9)+(2*4)+(1*7)=158
158 % 10 = 8
So 135939-47-8 is a valid CAS Registry Number.

135939-47-8Downstream Products

135939-47-8Relevant articles and documents

A new and versatile synthesis of 3-substituted oxetan-3-yl methyl alcohols

Boyd, Scott,Davies, Christopher D.

, p. 4117 - 4119 (2014/07/22)

We have developed a novel route for the efficient synthesis of pharmaceutically significant 3-substituted oxetan-3-yl methyl alcohols starting from readily available malonates. The synthesis harnesses the diversity of malonate chemistry and allows access to a range of oxetanes, which exemplifies the versatility of this procedure.

A new and versatile synthesis of 3-substituted oxetan-3-yl methyl alcohols

Boyd, Scott,Davies, Christopher D.

, p. 4117 - 4119 (2015/02/19)

We have developed a novel route for the efficient synthesis of pharmaceutically significant 3-substituted oxetan-3-yl methyl alcohols starting from readily available malonates. The synthesis harnesses the diversity of malonate chemistry and allows access to a range of oxetanes, which exemplifies the versatility of this procedure.

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