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141694-26-0

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141694-26-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 141694-26-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,6,9 and 4 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 141694-26:
(8*1)+(7*4)+(6*1)+(5*6)+(4*9)+(3*4)+(2*2)+(1*6)=130
130 % 10 = 0
So 141694-26-0 is a valid CAS Registry Number.

141694-26-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name N-Methyl-α-oxo-3-phenylpropanamide

1.2 Other means of identification

Product number -
Other names N-Methyl-2-oxo-3-phenyl-propionamide

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:141694-26-0 SDS

141694-26-0Downstream Products

141694-26-0Relevant articles and documents

The photochemistry of N-p-toluenesulfonyl peptides: The peptide bond as an electron donor

Hill, Roger R.,Moore, Sharon A.,Roberts, David R.

, p. 1439 - 1446 (2008/02/01)

The scope of photobiological processes that involve absorbers within a protein matrix may be limited by the vulnerability of the peptide group to attack by highly reactive redox centers consequent upon electronic excitation. We have explored the nature of this vulnerability by undertaking comprehensive product analyses of aqueous photolysates of 12 N-p-toluene-sulfonyl peptides with systematically selected structures. The results indicate that degradation includes a major pathway that is initiated by intramolecular electron transfer in which the peptide bond serves as electron donor, and the data support the likelihood' of a relay process in dipeptide derivatives.

α-Keto Amides and 1,2-Diketones from N,N'-Dimethoxy-N,N'-dimethylethanediamide. A Synthetic and Mechanistic Investigation

Sibi, Mukund P.,Marvin, Mali,Sharma, Rajiv

, p. 5016 - 5023 (2007/10/03)

N,N'-Dimethoxy-N,N'-dimethylethanediamide (1), a 1,2-dicarbonyl synthon prepared from oxalyl chloride, undergoes nucleophilic displacements with Grignard reagents to provide α-keto amides 2-12 in 28-90percent yields.The synthon also undergoes double nucleophilic displacements with organolithium reagents to furnish symmetrical 1,2-diketones 15-23 in 15-84percent yields.A mechanism accounting for all the products from the reaction of 1 with nucleophiles has been proposed.Several control experiments were carried out to support the proposed mechanism.

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