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Butyl 4-(4-chlorophenyl)-4-oxobutanoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

340283-98-9

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340283-98-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 340283-98-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,0,2,8 and 3 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 340283-98:
(8*3)+(7*4)+(6*0)+(5*2)+(4*8)+(3*3)+(2*9)+(1*8)=129
129 % 10 = 9
So 340283-98-9 is a valid CAS Registry Number.

340283-98-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name butyl 4-(4-chlorophenyl)-4-oxobutanoate

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

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:340283-98-9 SDS

340283-98-9Relevant academic research and scientific papers

2-Phenyl-imidazo[1,2-a]pyridine compounds containing hydrophilic groups as potent and selective ligands for peripheral benzodiazepine receptors: Synthesis, binding affinity and electrophysiological studies

Denora, Nunzio,Laquintana, Valentino,Pisu, Maria Giuseppina,Dore, Riccardo,Murru, Luca,Latrofa, Andrea,Trapani, Giuseppe,Sanna, Enrico

experimental part, p. 6876 - 6888 (2009/12/25)

A series of imidazopyridine acetamides were synthesized to evaluate the effects of structural changes at both central (CBRs) and peripheral benzodiazepine receptors (PBRs). These changes include the introduction of polar substituents or ionizable function

Aryl γ-ketoesters as precursors for γ-butyrolactones in samarium(II) iodide-mediated reactions

Bradley,Williams,Blann,Holzapfel

, p. 203 - 209 (2007/10/03)

Various aryl γ-ketoesters were transformed into the corresponding substituted γ-lactones in good yield upon reaction with SmI2.

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