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CAS

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19056-49-6

2-(IODOMETHYL)-5-METHYLTETRAHYDROFURAN is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 19056-49-6 Structure

  • Basic information

    1. Product Name: 2-(IODOMETHYL)-5-METHYLTETRAHYDROFURAN
    2. Synonyms: 2-(IODOMETHYL)-5-METHYLTETRAHYDROFURAN
    3. CAS NO:19056-49-6
    4. Molecular Formula: C6H11IO
    5. Molecular Weight: 0
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 19056-49-6.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: 2-(IODOMETHYL)-5-METHYLTETRAHYDROFURAN(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(IODOMETHYL)-5-METHYLTETRAHYDROFURAN(19056-49-6)
    11. EPA Substance Registry System: 2-(IODOMETHYL)-5-METHYLTETRAHYDROFURAN(19056-49-6)

  • 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: 19056-49-6(Hazardous Substances Data)

19056-49-6 Usage

Chemical structure

A tetrahydrofuran ring with an iodomethyl group and a methyl group attached to it.

Usage

Commonly used as an intermediate in the synthesis of various organic compounds and pharmaceuticals.

Reactivity

Known for its ability to undergo various reactions, such as nucleophilic substitution and metal-catalyzed processes.

Versatility

Acts as a versatile building block for the production of complex organic molecules.

Potential applications

Studied for its potential use as a reagent in organic chemistry and as a precursor in the creation of functionalized heterocycles.

Hazardous nature

Considered hazardous and may pose health risks if not handled properly.

Check Digit Verification of cas no

The CAS Registry Mumber 19056-49-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,0,5 and 6 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 19056-49:
(7*1)+(6*9)+(5*0)+(4*5)+(3*6)+(2*4)+(1*9)=116
116 % 10 = 6
So 19056-49-6 is a valid CAS Registry Number.

19056-49-6SDS

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-(iodomethyl)-5-methyloxolane

1.2 Other means of identification

Product number -
Other names 2-Methyl-5-iodomethyl-tetrahydrofuran

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:19056-49-6 SDS

19056-49-6Downstream Products

19056-49-6Relevant articles and documents

Stereoselective synthesis of cis-2,5-disubstituted THFs: Application to adjacent bis-THF cores of annonaceous acetogenins

Fujioka, Hiromichi,Maehata, Ryota,Wakamatsu, Shintaro,Nakahara, Kenji,Hayashi, Tatsuya,Oki, Tomohiro

supporting information; experimental part, p. 1054 - 1057 (2012/04/10)

The iodocyclization of γ,δ-unsaturated alcohols in the presence of a silyl enol ether produced cis-2,5-disubstituted tetrahydrofurans in one pot via siloxy intermediates. N-Iodosuccinimide (NIS) effectively worked as an activator of the double bonds in th

Iodocyclization of olefinic t-butyl ethers: An easy stereocontrolled synthesis of cis-substituted tetrahydrofurans

Marek,Lefrancois,Normant

, p. 1747 - 1748 (2007/10/02)

The iodoalkoxylation of δ,ε olefinic t-butyl ethers leads, with a very high selectivity, to cis substituted tetrahydrofurans.

ALKOXY RADICALS IN ORGANIC SYNTHESIS. A NOVEL APPROACH TO SPIROKETALS

Kraus, George A.,Thurston, Jeff

, p. 4011 - 4014 (2007/10/02)

Photolysis of an unsaturated alcohol in the presence of HgO and iodine generates an alkoxy radical which can cyclize to form a five-membered ring ether.If a hemiketal is employed, a spiroketal can be formed in good yield.

STEREOCHEMISTRY OF THE IODOCYCLIZATION OF UNSATURATED ALCOHOLS

Gevaza, Yu. I.,Kupchik, I. P.,Staninets, V. I.

, p. 24 - 26 (2007/10/02)

The corresponding tetrahydrofuran derivatives were obtained by iodination of δ,ε-unsaturated alcohols containing substituents attached to the α-carbon atom.The effect of substituents on the stereochemistry of the products and the rate of iodination of the

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