Welcome to LookChem.com Sign In|Join Free
  • or
Cyclobutanecarboxylic acid, 1-methyl-, ethyl ester is a chemical compound that is commonly used as a flavoring agent and fragrance ingredient in the food and fragrance industries. It is also used as a solvent in various industries. Cyclobutanecarboxylic acid, 1-methyl-, ethyl ester is a clear, colorless liquid with a sweet, fruity odor and is considered to be relatively stable under normal conditions, but may react with strong oxidizing agents.

65338-28-5

Post Buying Request

65338-28-5 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

65338-28-5 Usage

Uses

Used in Food Industry:
Cyclobutanecarboxylic acid, 1-methyl-, ethyl ester is used as a flavoring agent for enhancing the taste and aroma of various food products. Its sweet, fruity odor makes it suitable for adding a pleasant flavor to different types of food items.
Used in Fragrance Industry:
In the fragrance industry, Cyclobutanecarboxylic acid, 1-methyl-, ethyl ester is used as a fragrance ingredient to create various scent profiles for perfumes, colognes, and other scented products. Its sweet, fruity odor contributes to the overall scent composition and provides a unique olfactory experience.
Used in Pharmaceutical Production:
Cyclobutanecarboxylic acid, 1-methyl-, ethyl ester is used in the production of pharmaceuticals and other chemical compounds. Its chemical properties make it a valuable component in the synthesis of various drugs and medicinal products.
Used in Solvent Applications:
In various industries, Cyclobutanecarboxylic acid, 1-methyl-, ethyl ester is used as a solvent for dissolving and mixing different substances. Its ability to dissolve a wide range of materials makes it a versatile solvent for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 65338-28-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,3,3 and 8 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 65338-28:
(7*6)+(6*5)+(5*3)+(4*3)+(3*8)+(2*2)+(1*8)=135
135 % 10 = 5
So 65338-28-5 is a valid CAS Registry Number.

65338-28-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 1-methylcyclobutane-1-carboxylate

1.2 Other means of identification

Product number -
Other names Cyclobutanecarboxylic acid,1-methyl-,ethyl ester

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:65338-28-5 SDS

65338-28-5Relevant academic research and scientific papers

Discovery of Novel, Orally Bioavailable β-Amino Acid Azaindole Inhibitors of Influenza PB2

Farmer, Luc J.,Clark, Michael P.,Boyd, Michael J.,Perola, Emanuele,Jones, Steven M.,Tsai, Alice,Jacobs, Marc D.,Bandarage, Upul K.,Ledeboer, Mark W.,Wang, Tiansheng,Deng, Hongbo,Ledford, Brian,Gu, Wenxin,Duffy, John P.,Bethiel, Randy S.,Shannon, Dean,Byrn, Randal A.,Leeman, Joshua R.,Rijnbrand, Rene,Bennett, Hamilton B.,O’Brien, Colleen,Memmott, Christine,Nti-Addae, Kwame,Bennani, Youssef L.,Charifson, Paul S.

supporting information, p. 256 - 260 (2017/03/08)

In our efforts to develop novel small-molecule inhibitors for the treatment of influenza, we utilized molecular modeling and the X-ray crystal structure of the PB2 subunit of the influenza polymerase to optimize a series of acyclic β-amino acid inhibitors, highlighted by compound 4. Compound 4 showed good oral exposure in both rat and mouse. More importantly, it showed strong potency versus multiple influenza-A strains, including pandemic 2009 H1N1 and avian H5N1 strains and showed a strong efficacy profile in a mouse influenza model even when treatment was initiated 48 h after infection. Compound 4 offers good oral bioavailability with great potential for the treatment of both pandemic and seasonal influenza.

INHIBITORS OF INFLUENZA VIRUSES REPLICATION

-

Page/Page column 96-97, (2013/03/26)

Methods of inhibiting the replication of influenza viruses in a biological sample or patient, of reducing the amount of influenza viruses in a biological sample or patient, and of treating influenza in a patient, comprises administering to said biological sample or patient an effective amount of a compound represented by Structural Formula (I): or a pharmaceutically acceptable salt thereof, wherein the values of Structural Formula (I) are as described herein. A compound is represented by Structural Formula (I) or a pharmaceutically acceptable salt thereof, wherein the values of Structural Formula (I) are as described herein. A pharmaceutical composition comprises an effective amount of such a compound or pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier, adjuvant or vehicle.

INHIBITORS OF INFLUENZA VIRUSES REPLICATION

-

Paragraph 00265, (2014/01/08)

Compound according to Formula (I): or a pharmaceutically acceptable salt thereof, wherein the values of Structural Formula (I) are as described herein. A pharmaceutical composition comprises an effective amount of such a compound or pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier, adjuvant or vehicle. Uses of inhibiting the replication of influenza viruses in a biological sample or patient, of reducing the amount of influenza viruses in a biological sample or patient.

β-Arylation of carboxamides via iron-catalyzed C(sp3)-H bond activation

Shang, Rui,Ilies, Laurean,Matsumoto, Arimasa,Nakamura, Eiichi

supporting information, p. 6030 - 6032,3 (2013/05/22)

A 2,2-disubstituted propionamide bearing an 8-aminoquinolinyl group as the amide moiety can be arylated at the β-methyl position with an organozinc reagent in the presence of an organic oxidant, a catalytic amount of an iron salt, and a biphosphine ligand at 50 C. Various features of selectivity and reactivity suggest the formation of an organometallic intermediate via rate-determining C-H bond cleavage rather than a free-radical-type reaction pathway.

CYSTEINE PROTEASE INHIBITORS

-

Page/Page column 57, (2008/06/13)

A compound of the formula (II) wherein one of R1 and R2 is halo and the other is H or halo; R3 is -C1-C5 straight or branched chain, optionally fluorinated, alkyl or -CH2CR5Csub

ACYCLIC HYDRAZIDES AS CANNABINOID RECEPTOR MODULATORS

-

Page/Page column 48, (2010/11/08)

The acyclic hydrazides of the invention are antagonists and/or inverse agonists of the Cannabinoid-1 (CB1) receptor and are useful in the treatment, prevention and suppression of diseases mediated by the CB1 receptor. The compounds of the present inventio

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 65338-28-5