Welcome to LookChem.com Sign In|Join Free
  • or
2-benzyl-5-methyl-3-oxazolidine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1268151-04-7

Post Buying Request

1268151-04-7 Suppliers

Recommended suppliers

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

1268151-04-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1268151-04-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,8,1,5 and 1 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1268151-04:
(9*1)+(8*2)+(7*6)+(6*8)+(5*1)+(4*5)+(3*1)+(2*0)+(1*4)=147
147 % 10 = 7
So 1268151-04-7 is a valid CAS Registry Number.

1268151-04-7Downstream Products

1268151-04-7Relevant academic research and scientific papers

New insights into the formation of aroma-active strecker aldehydes from 3-oxazolines as transient intermediates

Granvogl, Michael,Beksan, Ersan,Schieberle, Peter

, p. 6312 - 6322 (2012)

2-Substituted-5-methyl-3-oxazolines, a novel class of aroma precursors that are able to release the respective Strecker aldehydes by hydrolysis, were identified. Hydrolysis can take place after the addition of water or with human saliva during mastication, respectively. 2-Isobutyl-, 2-sec-isobutyl-, 2-isopropyl, and 2-benzyl-5-methyl-3-oxazolines were synthesized and structurally identified by means of gas chromatography-mass spectrometry (GC-MS) in the electron impact mode and in the chemical ionization mode as well as by one- and two-dimensional NMR experiments. With these compounds at hand, a variety of stability experiments were performed using headspace-GC-MS or proton transfer reaction-MS techniques on the basis of stable isotope dilution assays, proving the ability to release the respective Strecker aldehydes was dependent on the pH value as well as on the hydrolysis time. After the addition of water at 37 °C, for example, >70 mol % of 3-methylbutanal or >40 mol % of phenylacetaldehyde was liberated from a solution of 2-isobutyl-5-methyl-3- oxazoline or 2-benzyl-5-methyl-3-oxazoline, respectively, after 5 min. Furthermore, the presence of 2-isobutyl-5-methyl-3-oxazoline in dark chocolate containing 70% cocoa was proven by GC-MS.

USE OF OXAZOLINES AS AROMA/FLAVOUR PRECURSORS

-

Page/Page column 38-40, (2013/10/21)

The present invention relates to compounds based on an oxazoline moiety which liberate Strecker aldehydes under mild and controllable conditions. In addition the invention relates to food products comprising such compounds, and uses of such compounds.

Use of oxazolines as aroma/flavour precursors

-

Paragraph 0102; 0103, (2013/10/21)

The present invention relates to compounds based on an oxazoline moiety which liberate Strecker aldehydes under mild and controllable conditions. In addition the invention relates to food products comprising such compounds, and uses of such compounds.

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 1268151-04-7