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Benzamide, N-(2-hydroxy-3-oxo-1,4,6-cycloheptatrien-1-yl)-, also known as 2-hydroxy-3-oxo-1,4,6-cycloheptatrien-1-yl-N-benzamide, is a complex organic compound with the molecular formula C14H11NO3. It is a derivative of benzamide, featuring a cycloheptatrienyl group with a hydroxyl and a carbonyl group attached to the nitrogen atom. Benzamide, N-(2-hydroxy-3-oxo-1,4,6-cycloheptatrien-1-yl)- is characterized by its unique structure, which includes a seven-membered aromatic ring with alternating double bonds, a hydroxyl group, and a carbonyl group. It is an important intermediate in the synthesis of various pharmaceuticals and agrochemicals due to its reactive functional groups and potential for further chemical modification. The compound's properties, such as solubility and reactivity, can be influenced by the presence of these functional groups, making it a versatile building block in organic synthesis.

2154-88-3

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2154-88-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2154-88-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,5 and 4 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2154-88:
(6*2)+(5*1)+(4*5)+(3*4)+(2*8)+(1*8)=73
73 % 10 = 3
So 2154-88-3 is a valid CAS Registry Number.

2154-88-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(2-hydroxy-3-oxocyclohepta-1,4,6-trien-1-yl)benzamide

1.2 Other means of identification

Product number -
Other names 3-Benzamidotropolone

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:2154-88-3 SDS

2154-88-3Relevant academic research and scientific papers

Reactions of 3-Aminotropolone with Acyl Halides. Formation of 8H-Cycloheptoxazol-8-ones

Imafuku, Kimiaki,Furuya, Miki,Jin, Zhong-Tian

, p. 1055 - 1056 (2007/10/02)

3-Aminotropolone (1) reacted with acetyl chloride and propionic chloride to give 2-methyl- and 2-ethyl-8H-cycloheptoxazol-8-ones (2a and 2b), respectively.The reaction with benzoyl chloride and phenylacetyl chloride gave N-acylated and N,O-diacylated 3

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