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165253-31-6

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165253-31-6 Usage

Description

(TETRAHYDROFURAN-3-YL)METHANAMINE is an organic compound that serves as a crucial intermediate in the chemical synthesis process. It is characterized by its unique molecular structure, which includes a tetrahydrofuran ring and an amine group attached to a methylene bridge. (TETRAHYDROFURAN-3-YL)METHANAMINE is known for its role in the creation of various chemical products, particularly in the agricultural and pharmaceutical industries.

Uses

Used in Agricultural Industry:
(TETRAHYDROFURAN-3-YL)METHANAMINE is used as a synthetic intermediate for the production of Dinoteturan (D482100), a neonicotinoid insecticide. This insecticide is effective in controlling a wide range of pests that damage crops, making it a valuable component in modern agriculture. Its use contributes to increased crop yields and reduced reliance on less environmentally friendly pest control methods.
Used in Pharmaceutical Industry:
While the provided materials do not explicitly mention any pharmaceutical applications for (TETRAHYDROFURAN-3-YL)METHANAMINE, its role as a synthetic intermediate suggests that it may be involved in the development of other pharmaceutical products. Given its structural properties, it could potentially be used in the synthesis of various drugs, including those with applications in treating diseases or conditions that require targeted drug delivery or specific molecular interactions. Further research and development in this area could reveal additional uses for this compound within the pharmaceutical industry.

Flammability and Explosibility

Nonflammable

Synthesis

Tetrahydrofuran-3-yl)methanamine,has been achieved through Michael addition reaction of nitromethane to diethyl maleate in 6 steps with 45.5% total yield.

Check Digit Verification of cas no

The CAS Registry Mumber 165253-31-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,5,2,5 and 3 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 165253-31:
(8*1)+(7*6)+(6*5)+(5*2)+(4*5)+(3*3)+(2*3)+(1*1)=126
126 % 10 = 6
So 165253-31-6 is a valid CAS Registry Number.
InChI:InChI=1/C5H11NO/c6-3-5-1-2-7-4-5/h5H,1-4,6H2

165253-31-6 Well-known Company Product Price

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  • Aldrich

  • (736759)  3-(Aminomethyl)tetrahydrofuran  95%

  • 165253-31-6

  • 736759-250MG

  • 1,304.55CNY

  • Detail

165253-31-6SDS

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 (Tetrahydrofuran-3-yl)methanamine

1.2 Other means of identification

Product number -
Other names oxolan-3-ylmethanamine

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:165253-31-6 SDS

165253-31-6Synthetic route

3-cyanotetrahydrofuran
14631-44-8

3-cyanotetrahydrofuran

(tetrahydro-3-furanyl)methylamine
165253-31-6

(tetrahydro-3-furanyl)methylamine

Conditions
ConditionsYield
With hydrogen In tert-butyl alcohol at 50 - 55℃; under 1125.11 Torr; for 6h; Solvent; Temperature; Pressure;93%
With palladium on activated charcoal; hydrogen In isopropyl alcohol at 70℃; under 7500.75 - 30003 Torr; for 5h; Reagent/catalyst; Solvent; Temperature; Pressure; Autoclave;92%
With ammonium hydroxide; hydrogen at 100℃; under 7500.75 Torr; for 4h; Autoclave;85%
With ammonium hydroxide; hydrogen at 110℃; under 18751.9 Torr; for 5h; Autoclave;62%
With hydrogen; nickel In tert-butyl alcohol at 50℃; under 380.026 Torr; for 10h; Autoclave;95 g
3-(nitromethyl)tetrahydrofuran

3-(nitromethyl)tetrahydrofuran

(tetrahydro-3-furanyl)methylamine
165253-31-6

(tetrahydro-3-furanyl)methylamine

Conditions
ConditionsYield
With hydrogen In methanol at 20℃; under 15001.5 Torr; for 2h; Reagent/catalyst; Pressure;99.4%
With palladium 10% on activated carbon; hydrogen In methanol at 20℃; under 760.051 Torr; for 6h;99%
With palladium 10% on activated carbon; hydrogen In methanol at 20℃; under 750.075 Torr; for 2h;95%
tetrahydrofuran-3-carboxaldehyde
79710-86-4

tetrahydrofuran-3-carboxaldehyde

(tetrahydro-3-furanyl)methylamine
165253-31-6

(tetrahydro-3-furanyl)methylamine

Conditions
ConditionsYield
With ammonia; hydrogen In methanol at 60℃; under 30003 Torr; for 12h; Pressure; Reagent/catalyst; Temperature;99.5%
With hydrogen In methanol at 60℃; under 26252.6 Torr; for 8.5h; Time; Autoclave; Inert atmosphere; Large scale;98.2%
With hydroxyapatite; ammonia; hydrogen In ethanol at 60℃; under 750.075 - 7500.75 Torr; for 3h; Autoclave; Large scale;95%

165253-31-6Relevant articles and documents

Chemoselective and Tandem Reduction of Arenes Using a Metal–Organic Framework-Supported Single-Site Cobalt Catalyst

Akhtar, Naved,Begum, Wahida,Chauhan, Manav,Manna, Kuntal,Newar, Rajashree,Rawat, Manhar Singh

supporting information, (2022/01/19)

The development of heterogeneous, chemoselective, and tandem catalytic systems using abundant metals is vital for the sustainable synthesis of fine and commodity chemicals. We report a robust and recyclable single-site cobalt-hydride catalyst based on a porous aluminum metal–organic framework (DUT-5 MOF) for chemoselective hydrogenation of arenes. The DUT-5 node-supported cobalt(II) hydride (DUT-5-CoH) is a versatile solid catalyst for chemoselective hydrogenation of a range of nonpolar and polar arenes, including heteroarenes such as pyridines, quinolines, isoquinolines, indoles, and furans to afford cycloalkanes and saturated heterocycles in excellent yields. DUT-5-CoH exhibited excellent functional group tolerance and could be reusable at least five times without decreased activity. The same MOF-Co catalyst was also efficient for tandem hydrogenation–hydrodeoxygenation of aryl carbonyl compounds, including biomass-derived platform molecules such as furfural and hydroxymethylfurfural to cycloalkanes. In the case of hydrogenation of cumene, our spectroscopic, kinetic, and density functional theory (DFT) studies suggest the insertion of a trisubstituted alkene intermediate into the Co–H bond occurring in the turnover limiting step. Our work highlights the potential of MOF-supported single-site base–metal catalysts for sustainable and environment-friendly industrial production of chemicals and biofuels.

Synthesis method for 3-aminomethyl tetrahydrofuran

-

Paragraph 0054; 0058; 0061; 0065-0066; 0070-0071; 0075, (2020/07/14)

The invention provides a synthetic method for 3-aminomethyl tetrahydrofuran. A target product, namely the 3-aminomethyl tetrahydrofuran is prepared by taking 2,5-dihydrofuran as an initial raw material. In the whole synthesis process, the synthesis method has the advantages of green and environmentally-friendly used raw materials, mild and conveniently-controllable reaction conditions, safe production, low risk, simple process, high yield, and more applicability to industrial production.

The invention relates to a benzofuran as raw materials for the synthesis of 3 - amino methyl tetrahydrofuran (by machine translation)

-

, (2019/07/04)

The invention relates to a benzofuran as raw materials for the synthesis of 3 - amino methyl tetrahydrofuran, relates to the technical field of the synthesis intermediate for agricultural chemicals, to benzofuran as raw materials, obtained by the oxidation of the open loop 1, 4 - butene dialdehyde, and nitromethane by Michael addition, sodium borohydride reduction, dehydration cyclization and catalytic hydrogenation to five-step reaction to obtain 3 - amino methyl tetrahydrofuran. The present invention provides a benzofuran as raw materials for the synthesis of 3 - amino methyl tetrahydrofuran, the method cheap price of raw materials, synthetic route is short, low production cost, is suitable for mass production. (by machine translation)

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