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CAS

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17515-73-0

ETHYL 5-METHYL-2-(TRIFLUOROMETHYL)-3-FUROATE is a complex organic compound characterized by a trifluoromethyl group attached to the second position of the furoate molecule, which provides a strong and stable chemical structure. This synthesized molecule is primarily used for research applications and in the production of other complex molecules.

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  • 17515-73-0 Structure

  • Basic information

    1. Product Name: ETHYL 5-METHYL-2-(TRIFLUOROMETHYL)-3-FUROATE
    2. Synonyms: ETHYL 5-METHYL-2-(TRIFLUOROMETHYL)-3-FUROATE;Ethyl 5-methyl-2-(trifluoromethyl)-3-furoate 97%;Ethyl5-methyl-2-(trifluoromethyl)-3-furoate97%;3-Furancarboxylic acid,5-methyl-2-(trifluoromethyl)-, ethyl ester
    3. CAS NO:17515-73-0
    4. Molecular Formula: C9H9F3O3
    5. Molecular Weight: 222.16
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 17515-73-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 55°C 0,3mm
    3. Flash Point: 101.5°C
    4. Appearance: /
    5. Density: 1.259g/cm3
    6. Refractive Index: N/A
    7. Storage Temp.: 2-8°C(protect from light)
    8. Solubility: N/A
    9. CAS DataBase Reference: ETHYL 5-METHYL-2-(TRIFLUOROMETHYL)-3-FUROATE(CAS DataBase Reference)
    10. NIST Chemistry Reference: ETHYL 5-METHYL-2-(TRIFLUOROMETHYL)-3-FUROATE(17515-73-0)
    11. EPA Substance Registry System: ETHYL 5-METHYL-2-(TRIFLUOROMETHYL)-3-FUROATE(17515-73-0)

  • Safety Data

    1. Hazard Codes: Xi
    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: 17515-73-0(Hazardous Substances Data)

17515-73-0 Usage

Uses

Used in Organic Synthesis:
ETHYL 5-METHYL-2-(TRIFLUOROMETHYL)-3-FUROATE is used as a building block for the synthesis of more complex organic molecules, due to its stable and versatile chemical structure.
Used in Pharmaceutical Research:
ETHYL 5-METHYL-2-(TRIFLUOROMETHYL)-3-FUROATE is used as a research compound in the development of new pharmaceuticals, potentially contributing to the discovery of novel drug candidates.
Used in Chemical Research:
ETHYL 5-METHYL-2-(TRIFLUOROMETHYL)-3-FUROATE is used as a research tool in various fields of chemistry, such as studying reaction mechanisms or exploring new synthetic pathways.
Note: Since the provided materials do not contain specific information about the toxicity or environmental and human effects of ETHYL 5-METHYL-2-(TRIFLUOROMETHYL)-3-FUROATE, it is important to handle this compound with caution and follow appropriate safety protocols.

Check Digit Verification of cas no

The CAS Registry Mumber 17515-73-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,5,1 and 5 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 17515-73:
(7*1)+(6*7)+(5*5)+(4*1)+(3*5)+(2*7)+(1*3)=110
110 % 10 = 0
So 17515-73-0 is a valid CAS Registry Number.

17515-73-0SDS

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 ethyl 5-methyl-2-(trifluoromethyl)furan-3-carboxylate

1.2 Other means of identification

Product number -
Other names ethyl 5-methyl-2-(trifluoromethyl)-3-furancarboxylate

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:17515-73-0 SDS

17515-73-0Relevant articles and documents

AMINOETHANOL DERIVATIVES

-

Page/Page column 125, (2010/11/30)

The present invention provides a pharmaceutical agent having cholesteryl ester transfer protein inhibitory action and useful as a blood lipid lowering agent and the like. The present invention relates to a compound represented by the formula wherein Ar1 is an aromatic ring group optionally having substituents, Ar2 is an aromatic ring group having substituents, OR'' is an optionally protected hydroxyl group, R is an acyl group, R' is a hydrogen atom or a hydrocarbon group optionally having substituents, or a salt thereof, and a pharmaceutical composition containing a compound of the formula (I) or a salt thereof or a prodrug thereof.

Trifluoromethylated Furans via Iodocyclisation of γ-Unsaturated Ethyl Trifluoroacetoacetates

Begue, Jean-Pierre,Bonnet-Delpon, Daniele,Dogbeavou, Romain,Ourevitch, Michele

, p. 2787 - 2792 (2007/10/02)

Under iodoetherification conditions, γ-unsaturated ethyl trifluoroacetoacetates 1a-c exhibit a specific reactivity.Conditions were found for the synthesis of cyclic iodo hemiketals 2a-c and for their subsequent conversion into either α-trifluoromethylated

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