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3041-15-4

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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 articles and documents

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.

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