Welcome to LookChem.com Sign In|Join Free
  • or
11-methyloxacycloundecan-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

3041-15-4

Post Buying Request

3041-15-4 Suppliers

Recommended suppliers

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

3041-15-4 Usage

Chemical family

Oxacyclic compounds

Type of compound

Saturated heterocyclic ketone

Ring size

12-membered ring

Structural feature

Methyl group attached to the carbon at position 11

Molecular weight

198.30 g/mol

Applications

Synthesis of pharmaceuticals and organic compounds

Intermediate use

Production of fragrances and flavoring agents

Importance

Versatile building block in organic chemistry and drug development

Check Digit Verification of cas no

The CAS Registry Mumber 3041-15-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,0,4 and 1 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 3041-15:
(6*3)+(5*0)+(4*4)+(3*1)+(2*1)+(1*5)=44
44 % 10 = 4
So 3041-15-4 is a valid CAS Registry Number.

3041-15-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 11-methyl-oxacycloundecan-2-one

1.2 Other means of identification

Product number -
Other names Oxacycloundecan-2-one,11-methyl

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:3041-15-4 SDS

3041-15-4Relevant academic research and scientific papers

From Azido Acids to Macrolactams and Macrolactones

Bartra, Marti,Bou, Valenti,Garcia, Jordi,Urpi, Felix,Vilarrasa, Jaume

, p. 270 - 272 (2007/10/02)

A new method is reported for the conversion of azido acids into lactams, via thioester formation and in situ azide reduction and cyclisation under high-dilution conditions; since the quantitative conversion of macrolactams to macrolactones has been shown to be feasible, this results in an indirect, alternative macrolactonisation procedure.

LIPASE CATALYZED SYNTHESIS OF MACROCYCLIC LACTONES IN ORGANIC SOLVENTS

Makita, Atushi,Nihira, Takuya,Yamada, Yasuhiro

, p. 805 - 808 (2007/10/02)

A new method for the preparation of macrocyclic lactones from ω-hydroxyacid methyl esters is described.The approach utilizes intramolecular transesterification catalyzed by lipase in organic solvents.The procedure is also applicable to the synthesis of asymmetric lactones.

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 3041-15-4