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Pentanamide, 4-oxo- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

22377-14-6

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22377-14-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 22377-14-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,3,7 and 7 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 22377-14:
(7*2)+(6*2)+(5*3)+(4*7)+(3*7)+(2*1)+(1*4)=96
96 % 10 = 6
So 22377-14-6 is a valid CAS Registry Number.

22377-14-6SDS

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-oxopentanamide

1.2 Other means of identification

Product number -
Other names Laevulinsaeureamid

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:22377-14-6 SDS

22377-14-6Downstream Products

22377-14-6Relevant academic research and scientific papers

Zinc carbenoid-mediated chain extension of β-keto amides

Hilgenkamp, Ramona,Zercher, Charles K

, p. 8793 - 8800 (2007/10/03)

The reaction of β-keto amides with ethyl(iodomethyl)zinc provides access to a wide variety of γ-keto amides, including primary, secondary, and tertiary amides. Although the reaction of α-substituted β-keto amides are in many cases unsatisfactory, the method can be applied to a broad spectrum of substrates that possess imide and olefinic functionality.

Study of photochemical addition of acyl radical to electron-deficient olefins

Macias,Molinillo,Massanet,Rodriguez-Luis

, p. 3345 - 3352 (2007/10/02)

The photochemical addition of acyl radical to electron-deficient olefins is studied. The scope of the reaction, the mechanism, the role that molecular oxygen plays, the influence of steric effects, and the side reaction that take place are discussed. The reaction was carried out using a range of electron-withdrawing substituents (ketones, amides, lactones, nitrile and esters) with good yields of the corresponding photoadduct in all cases.

An efficient and mild entry to 1,4-dicarbonyl compounds via photochemical addition of acyl radical to electron-deficient olefins

Macias, Francisco A.,Molinillo, Jose Maria G.,Collado, Isidro G.,Massanet, Guillermo M.,Rodriguez-Luis, Francisco

, p. 3063 - 3066 (2007/10/02)

Photoehcmical addition of acetaldehyde to electron-deficient olefins in the presence of molecular oxygen provides an efficient and mild method for the synthesis of 1,4-functionallzed compounds. Some considerations about the mechanism and the substituent effects are outlined.

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