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N-[(3E)-3-(hydroxyimino)-1-phenylbutan-2-yl]acetamide is a complex organic compound with the molecular formula C12H16N2O2. It is characterized by a 3-(hydroxyimino)-1-phenylbutan-2-yl group, which is in the E configuration, indicating the geometric arrangement of the double bond. This molecule features a hydroxyimino group, which is a functional group containing a hydroxyl group and an imino group, and an acetamide group, which is an amide derived from acetic acid. The compound is known for its potential applications in pharmaceuticals and as a chemical intermediate. It is important to note that the specific properties, reactivity, and uses of N-[(3E)-3-(hydroxyimino)-1-phenylbutan-2-yl]acetamide can vary depending on its context and the conditions under which it is studied or applied.

6955-09-5

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6955-09-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6955-09-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,5 and 5 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6955-09:
(6*6)+(5*9)+(4*5)+(3*5)+(2*0)+(1*9)=125
125 % 10 = 5
So 6955-09-5 is a valid CAS Registry Number.

6955-09-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[(3Z)-3-hydroxyimino-1-phenylbutan-2-yl]acetamide

1.2 Other means of identification

Product number -
Other names -

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

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More Details:6955-09-5 SDS

6955-09-5Relevant academic research and scientific papers

UEBERFUEHRUNG VON N-ACYLAMINOSAEUREN IN ENAMINE DURCH BECKMAN-FRAGMENTIERUNG VON α-ACYLAMINOKETOXIMEN

Redeker, Ursula,Engel, Norbert,Steglich, Wolfgang

, p. 4263 - 4264 (2007/10/02)

A three-step sequence is described which permits conversion of N-acylamino acids and N-acylpeptides into the corresponding enamides.

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