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1178131-96-8

4-(4-methoxyphenylamino)tetrahydrofuran-3-ol is a chemical compound characterized by a tetrahydrofuran ring, an amino group attached to a phenyl group, and a methoxy substituent. It is an organic compound with potential pharmaceutical applications due to its structural features.
Used in Pharmaceutical Industry:
4-(4-methoxyphenylamino)tetrahydrofuran-3-ol is used as a building block for the synthesis of various pharmaceutical compounds, owing to its tetrahydrofuran derivative structure and potential biological activity.
4-(4-methoxyphenylamino)tetrahydrofuran-3-ol is used as a potential drug candidate for drug discovery and development, due to the presence of the methoxyphenylamino group that may allow for interactions with biological targets.
Note: The specific applications and reasons for the uses of 4-(4-methoxyphenylamino)tetrahydrofuran-3-ol are not provided in the materials. The above uses are inferred based on the general potential of such compounds in the pharmaceutical industry. Further research and studies are necessary to fully understand its potential uses and biological activity.

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  • 1178131-96-8 Structure

  • Basic information

    1. Product Name: 4-(4-methoxyphenylamino)tetrahydrofuran-3-ol
    2. Synonyms: 4-(4-methoxyphenylamino)tetrahydrofuran-3-ol;Tetrahydro-4-[(4-methoxyphenyl)amino]-3-furanol
    3. CAS NO:1178131-96-8
    4. Molecular Formula: C11H15NO3
    5. Molecular Weight: 209.2417
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1178131-96-8.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.262
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 4-(4-methoxyphenylamino)tetrahydrofuran-3-ol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-(4-methoxyphenylamino)tetrahydrofuran-3-ol(1178131-96-8)
    11. EPA Substance Registry System: 4-(4-methoxyphenylamino)tetrahydrofuran-3-ol(1178131-96-8)

  • 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: 1178131-96-8(Hazardous Substances Data)

1178131-96-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1178131-96-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,7,8,1,3 and 1 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1178131-96:
(9*1)+(8*1)+(7*7)+(6*8)+(5*1)+(4*3)+(3*1)+(2*9)+(1*6)=158
158 % 10 = 8
So 1178131-96-8 is a valid CAS Registry Number.

1178131-96-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(4-methoxyanilino)oxolan-3-ol

1.2 Other means of identification

Product number -
Other names 4-(4-methoxyphenylamino)tetrahydrofuran-3-ol

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:1178131-96-8 SDS

1178131-96-8Downstream Products

1178131-96-8Relevant articles and documents

Enantioselective synthesis of heterocyclic β-aminoalcohols catalysed by a samarium iodo binaphtholate

Martin, Myriam,Bezzenine-Lafollee, Sophie,Gil, Richard,Collin, Jacqueline

, p. 2598 - 2605 (2007)

Enantioselective aminolysis of meso-epoxides including a heterocycle catalysed by a samarium iodo binaphtholate has been studied. New β-amino alcohols have been isolated with enantiomeric excesses up to 70%.

Synthesis of rare earth catalysts and their applications for enantioselective synthesis of heterocyclic β-amino alcohols

Martin, Myriam,El Hellani, Ahmad,Yang, Jing,Collin, Jacqueline,Bezzenine-Lafollee, Sophie

experimental part, p. 9801 - 9808 (2012/01/13)

A new family of chiral lanthanide complexes derived from (R)-binaphthol has been synthesized by a one-pot procedure using only commercially available substrates. These complexes were evaluated for the aminolysis of meso-epoxides and proved to be efficient enantioselective catalysts. The samarium complex coordinated by two (R)-binaphthoxide ligands was the most enantioselective catalyst of this series. β-Amino alcohols including heterocycles have been isolated with enantiomeric excesses up to 84%.

Insight into the structure of the precatalyst and active species for samarium iodo binaphtholate catalysed aminolysis of epoxides

Martin, Myriam,Bezzenine, Sophie,Collin, Jacqueline

experimental part, p. 1722 - 1729 (2010/10/20)

Samarium iodo binaphtholate is an efficient Lewis acid catalyst for the enantioselective carbon-nitrogen bond formation such as aza-Michael reactions and the aminolysis of epoxides allowing highly enantioenriched aminoalcohols and aminoacids building bloc

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