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N-(2-acetyl-5-chloro-phenyl)formamide is a chemical compound with the molecular formula C9H8ClNO2. It is an organic compound that features a formamide functional group attached to a 2-acetyl-5-chlorophenyl ring. This molecule is characterized by a chlorine atom at the 5-position and an acetyl group (a two-carbon acyl group) at the 2-position of the phenyl ring. The formamide group, which consists of a carbonyl group (C=O) bonded to an amino group (-NH2), is attached to the phenyl ring through the nitrogen atom. N-(2-acetyl-5-chloro-phenyl)formamide may have potential applications in the synthesis of pharmaceuticals or other organic compounds due to its unique structure and reactivity.

6938-28-9

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6938-28-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6938-28-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,3 and 8 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6938-28:
(6*6)+(5*9)+(4*3)+(3*8)+(2*2)+(1*8)=129
129 % 10 = 9
So 6938-28-9 is a valid CAS Registry Number.
InChI:InChI=1/C9H8ClNO2/c1-6(13)8-3-2-7(10)4-9(8)11-5-12/h2-5H,1H3,(H,11,12)

6938-28-9SDS

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-(2-acetyl-5-chlorophenyl)formamide

1.2 Other means of identification

Product number -
Other names formic acid-(2-acetyl-5-chloro-anilide)

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:6938-28-9 SDS

6938-28-9Relevant academic research and scientific papers

Cyclization reactions of 2-isothiocyanatophenyl ketones giving 4-hydroxyquinoline-2(1H)-thiones and 4-alkylidene-1,4-dihydro-3,1-benzoxazine-2- thiones

Kobayashi, Kazuhiro,Komatsu, Toshihide,Fukamachi, Shuhei,Konishi, Hisatoshi

experimental part, p. 2097 - 2104 (2011/04/24)

2-Isothiocyanatophenyl methyl ketones, generated in situ by treatment of 2-isocyanophenyl methyl ketones with sulfur in the presence of a catalytic amount of selenium and excess triethylamine, underwent electrocyclic reaction (ECR) via their enolate forms

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