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CAS

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14739-10-7

4-(2,2-dimethyl-1,3-dioxolan-4-yl)butan-1-ol is a chemical compound that belongs to the class of alcohols. It is characterized by a butyl chain with a hydroxyl group and a dioxolane ring, which imparts unique properties and reactivity to the molecule. This colorless liquid at room temperature is utilized in a variety of chemical and industrial applications.

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  • 14739-10-7 Structure

  • Basic information

    1. Product Name: 4-(2,2-dimethyl-1,3-dioxolan-4-yl)butan-1-ol
    2. Synonyms:
    3. CAS NO:14739-10-7
    4. Molecular Formula: C9H18O3
    5. Molecular Weight: 174.2374
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 14739-10-7.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 240.2°C at 760 mmHg
    3. Flash Point: 114.7°C
    4. Appearance: N/A
    5. Density: 0.982g/cm3
    6. Vapor Pressure: 0.00669mmHg at 25°C
    7. Refractive Index: 1.437
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 4-(2,2-dimethyl-1,3-dioxolan-4-yl)butan-1-ol(CAS DataBase Reference)
    11. NIST Chemistry Reference: 4-(2,2-dimethyl-1,3-dioxolan-4-yl)butan-1-ol(14739-10-7)
    12. EPA Substance Registry System: 4-(2,2-dimethyl-1,3-dioxolan-4-yl)butan-1-ol(14739-10-7)

  • 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: 14739-10-7(Hazardous Substances Data)

14739-10-7 Usage

Uses

Used in Chemical Synthesis:
4-(2,2-dimethyl-1,3-dioxolan-4-yl)butan-1-ol is used as a reagent in the synthesis of various organic compounds due to its unique structure and reactivity.
Used in Pharmaceutical Production:
In the pharmaceutical industry, 4-(2,2-dimethyl-1,3-dioxolan-4-yl)butan-1-ol is used as an intermediate in the production of certain medications, contributing to the development of new drugs.
Used as a Solvent:
4-(2,2-dimethyl-1,3-dioxolan-4-yl)butan-1-ol is utilized as a solvent in various chemical processes, providing a medium for reactions to occur.
While the potential hazards of 4-(2,2-dimethyl-1,3-dioxolan-4-yl)butan-1-ol have not been extensively studied, it is important to follow proper handling procedures and safety precautions when working with 4-(2,2-dimethyl-1,3-dioxolan-4-yl)butan-1-ol.

Check Digit Verification of cas no

The CAS Registry Mumber 14739-10-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,7,3 and 9 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 14739-10:
(7*1)+(6*4)+(5*7)+(4*3)+(3*9)+(2*1)+(1*0)=107
107 % 10 = 7
So 14739-10-7 is a valid CAS Registry Number.

14739-10-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(2,2-dimethyl-1,3-dioxolan-4-yl)butan-1-ol

1.2 Other means of identification

Product number -
Other names 4-(4-hydroxybutyl)-2,2-dimethyl-1,3-dioxolane

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:14739-10-7 SDS

14739-10-7Relevant articles and documents

Dimethylboron Bromide and Diphenylboron Bromide: Cleavage of Acetals and Ketals

Guindon, Yvan,Yoakim, Christiane,Morton, Howard E.

, p. 3912 - 3920 (2007/10/02)

The cleavage of various acetal and ketal derivatives by the use of dialkyl- and diarylboron halides is described.Acetals and ketals readily react with dimethylboron bromide or diphenylboron bromide at -78 deg C to give the corresponding carbonyl compounds in excellent yield.Under similar reaction conditions MEM, MOM, and MTM ethers are smoothly converted to alcohols.Acetonides are also cleaved with dimethylboron bromide while THP and THF ethers and methyl glycosides react at room temperature.Mechanistic considerations of the cleavage reactions are presented.The chemoselective virtues of dimethylboron bromide are summarized.

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