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4-acetyl-5-methylhexanenitrile is an organic compound with the molecular formula C9H15NO. It is a colorless liquid with a fruity, apple-like odor. This chemical is primarily used as a flavoring agent in the food and beverage industry, as well as in the production of fragrances. It is synthesized through a series of chemical reactions, including the condensation of acetone with 2-methylbutanal and subsequent cyanoethylation. Due to its reactive nature, it is essential to handle 4-acetyl-5-methylhexanenitrile with care, following proper safety protocols.

34041-01-5

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34041-01-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 34041-01-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,0,4 and 1 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 34041-01:
(7*3)+(6*4)+(5*0)+(4*4)+(3*1)+(2*0)+(1*1)=65
65 % 10 = 5
So 34041-01-5 is a valid CAS Registry Number.

34041-01-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-acetyl-5-methylhexanenitrile

1.2 Other means of identification

Product number -
Other names 5-Methyl-4-acetyl-hexansaeure-nitril

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:34041-01-5 SDS

34041-01-5Downstream Products

34041-01-5Relevant academic research and scientific papers

Stereoselective synthesis of the bicyclo[5.3.0]decane portion of the diterpene antibiotic guanacastepene using a pyrylium-ylide [5+2] cycloaddition reaction

Magnus, Philip,Waring, Michael J.,Ollivier, Cyril,Lynch, Vince

, p. 4947 - 4950 (2007/10/03)

Treatment of 14 with Ac2O/Et3N resulted in [5+2] cyclization to give 2, which was further elaborated into 20, thus establishing the required stereochemistry in the top-half of guanacastepene 1.

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