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2911-38-8

[(Cyclohexylideneamino)oxy](phenylamino)methanone is a complex organic compound with the chemical formula C14H16N2O2. It is a derivative of methanone, featuring a cyclohexylidene group attached to the nitrogen atom, and a phenyl group attached to the other nitrogen atom. [(cyclohexylideneamino)oxy](phenylamino)methanone is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity. It is a white crystalline solid and is typically used as an intermediate in the production of other chemicals. The compound's properties, such as its solubility and stability, can vary depending on the specific conditions under which it is synthesized and stored.

2911-38-8

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2911-38-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2911-38-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,1 and 1 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2911-38:
(6*2)+(5*9)+(4*1)+(3*1)+(2*3)+(1*8)=78
78 % 10 = 8
So 2911-38-8 is a valid CAS Registry Number.

2911-38-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (cyclohexylideneamino) N-phenylcarbamate

1.2 Other means of identification

Product number -
Other names Cyclohexanon-(O-phenylcarbamoyl-oxim)

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:2911-38-8 SDS

2911-38-8Upstream product

2911-38-8Downstream Products

2911-38-8Relevant articles and documents

Reactivity of bis(arylcarbamoyl)-N-arylphenacylamine oximes. Synthesis of 1,3-dihydroimidazol-2-ones and N-unsubstituted O- arylcarbamoylhydroxylamines

Coskun, Necdet

, p. 475 - 484 (1999)

N-Arylphenacylamine oximes 1 reacted with aryl isocyanates in refluxing benzene to give bis(arylcarbamoyl)-N-arylphenacylamine oximes 2 in good yields. Compounds 2 reacted with equimolar amount of TsOH.H2O in THF at room temperature to give imidazol-2-ones 5 and O-arylcarbamoylhydroxylammonium tosylates 6 in high yields. Compounds 2 were heated under vacuum to induce Beckmann fragmentation but the resulting products were 1,3,4-triaryl-1,3- dihydroimidazol-2-ones 5 instead of the expected 1,3-diazetidinones 4.

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