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1,3-Dioxolane, 2-(5-hexynyl)- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 67100-12-3 Structure
  • Basic information

    1. Product Name: 1,3-Dioxolane, 2-(5-hexynyl)- (9CI)
    2. Synonyms: 1,3-Dioxolane, 2-(5-hexynyl)- (9CI)
    3. CAS NO:67100-12-3
    4. Molecular Formula: C9H14O2
    5. Molecular Weight: 154.21
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 67100-12-3.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: 1,3-Dioxolane, 2-(5-hexynyl)- (9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,3-Dioxolane, 2-(5-hexynyl)- (9CI)(67100-12-3)
    11. EPA Substance Registry System: 1,3-Dioxolane, 2-(5-hexynyl)- (9CI)(67100-12-3)
  • 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: 67100-12-3(Hazardous Substances Data)

67100-12-3 Usage

Chemical class

Dioxolane compounds

Explanation

A class of organic compounds containing a five-membered ring with two oxygen atoms and an additional functional group.

Explanation

A terminal alkyne with a six-carbon chain attached to the dioxolane ring.

Explanation

Primarily used as a building block in the synthesis of various organic compounds, including pharmaceuticals, agrochemicals, and materials.

Explanation

The specific arrangement of atoms and functional groups in 1,3-Dioxolane, 2-(5-hexynyl)(9CI) makes it useful for creating new chemical compounds and products.

Explanation

As with any chemical, it is essential to follow safety guidelines and precautions when working with 1,3-Dioxolane, 2-(5-hexynyl)(9CI) to ensure the safety of workers and the environment.

Structure

Contains a hexynyl group

Application

Research and industrial use

Unique structure

Valuable for new chemical compound development

Safety precautions

Proper handling required

Check Digit Verification of cas no

The CAS Registry Mumber 67100-12-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,1,0 and 0 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 67100-12:
(7*6)+(6*7)+(5*1)+(4*0)+(3*0)+(2*1)+(1*2)=93
93 % 10 = 3
So 67100-12-3 is a valid CAS Registry Number.

67100-12-3SDS

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 2-Hex-5-ynyl-[1,3]dioxolane

1.2 Other means of identification

Product number -
Other names -

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:67100-12-3 SDS

67100-12-3Downstream Products

67100-12-3Relevant articles and documents

A New Methodology to Key Intermediates for Synthesizing Polyene Compounds

Ma, Dawei,Lu, Xiyan

, p. 6319 - 6330 (2007/10/02)

ω-Alkoxy-(2E,4E)-dienoates, ω-oxo-(2E,4E)-dienoates and δ-oxo-α,β:γ,δ-dienones were prepared according to a new methodology shown in scheme I.High yield and high stereoselectivity were achieved by using transition metal catalyzed isomerization of ynoates or ynones instead of using Wittig-Horner-wadsworth-Emmons reaction to constitute the diene moiety.The usefulness of this methodology was demonstrated by the preparation of important synthetic precursors to polyene compounds and natural products such as 10--(2E,4E)-decadienoates, methyl 8--(2E,4E)-octadienoate, methyl 10-benzyloxy-(2E,4E)-decadienoate, 6-oxo-(2E,4E)-tetradecadienal, methyl 8-oxo-(2E,4E)-octadienoate, and retrofractamide A.

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