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1186127-15-0

Ethyl 2-(5-Oxazolyl)benzoate, also known as ethyl anthranilate, is a chemical compound that is widely used in the fragrance and flavor industries. It is derived from benzoic acid and ethanol and is characterized by its sweet, floral odor. Ethyl anthranilate is recognized for its natural occurrence in certain fruits and flowers, which has led to its exploration as a potential insect repellent.
Used in Fragrance Industry:
Ethyl 2-(5-Oxazolyl)benzoate is used as a fragrance ingredient for its sweet, floral scent, contributing to the creation of perfumes, soaps, and other scented products.
Used in Flavor Industry:
In the flavor industry, Ethyl 2-(5-Oxazolyl)benzoate is used as a flavoring agent to impart grape and raspberry flavors to food and beverages.
Used in Insect Repellent Research:
Ethyl 2-(5-Oxazolyl)benzoate is studied as a potential insect repellent due to its natural presence in fruits and flowers, which may deter insects.
Ethyl 2-(5-Oxazolyl)benzoate has been deemed safe for use in consumer products by regulatory agencies, although it may cause mild skin and eye irritation in some individuals.

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  • 1186127-15-0 Structure

  • Basic information

    1. Product Name: Ethyl 2-(5-Oxazolyl)benzoate
    2. Synonyms: Ethyl 2-(5-Oxazolyl)benzoate;2-(5-oxazolyl) Benzoic acid ethyl ester
    3. CAS NO:1186127-15-0
    4. Molecular Formula: C12H11NO3
    5. Molecular Weight: 217.22064
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1186127-15-0.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: Ethyl 2-(5-Oxazolyl)benzoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: Ethyl 2-(5-Oxazolyl)benzoate(1186127-15-0)
    11. EPA Substance Registry System: Ethyl 2-(5-Oxazolyl)benzoate(1186127-15-0)

  • 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: 1186127-15-0(Hazardous Substances Data)

1186127-15-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1186127-15-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,8,6,1,2 and 7 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1186127-15:
(9*1)+(8*1)+(7*8)+(6*6)+(5*1)+(4*2)+(3*7)+(2*1)+(1*5)=150
150 % 10 = 0
So 1186127-15-0 is a valid CAS Registry Number.

1186127-15-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-(oxazol-5-yl)benzoate

1.2 Other means of identification

Product number -
Other names Ethyl 2-(5-Oxazolyl)benzoate

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:1186127-15-0 SDS

1186127-15-0Downstream Products

1186127-15-0Relevant articles and documents

Improvement of the Van Leusen reaction in the presence of β-cyclodextrin: A green and efficient synthesis of oxazoles in water

Rahimzadeh, Golnaz,Kianmehr, Ebrahim,Mahdavi, Mohammad

, p. 923 - 926 (2017/12/18)

An efficient approach for the synthesis of oxazoles through the Van Leusen reaction in the presence of β-cyclodextrin is described. In aqueous medium using β-cyclodextrin as a supramolecular catalyst, tosylmethyl isocyanide was deprotonated by triethylami

Synthesis of 2-TIPS-oxazol-5-ylboronic acid pinacol ester: efficient route to 5-(het)aryloxazoles via Suzuki cross-coupling reaction

Primas, Nicolas,Bouillon, Alexandre,Lancelot, Jean-Charles,Rault, Sylvain

experimental part, p. 6348 - 6353 (2009/12/04)

A facile synthetic route to the new 2-TIPS-oxazol-5-ylboronic acid pinacol ester was described herein. Its reactivity toward Suzuki cross-coupling reaction was studied to provide various 5-(het)aryloxazoles. A wide range of functions on the aryl moiety ar

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