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15386-84-2

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15386-84-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 15386-84-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,3,8 and 6 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 15386-84:
(7*1)+(6*5)+(5*3)+(4*8)+(3*6)+(2*8)+(1*4)=122
122 % 10 = 2
So 15386-84-2 is a valid CAS Registry Number.

15386-84-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 3-(4-chloroanilino)-3-oxopropanoate

1.2 Other means of identification

Product number -
Other names ethyl 3-(4-chloroanilino)-3-oxopropionate

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:15386-84-2 SDS

15386-84-2Relevant articles and documents

AlCl 3 -Mediated Synthesis of 4-Aryl-2-quinolone-3-carboxylates

Yang, Seung-Hye,Jo, Seohyun,Shin, Dongyun

, p. 1614 - 1619 (2017/08/11)

4-Aryl-2-quinolones are important skeletons from both chemical and medicinal viewpoints. We herein report the development of an efficient synthetic method for 3-substituted 4-aryl-2-quinolones. The key reaction in this process involves an AlCl 3/sub

INHIBITION OF INVERTEBRATES USING LIGANDS THAT MODULATE ECDYSONE RECEPTORS

-

Page/Page column 43, (2008/12/06)

The present invention relates to the use of N-substituted γ-methylene γ-lactams as non- steroidal ligands for modulating ecdysone receptors generally (resulting in controlled insect growth) and, in particular, ecdysone receptors of the Australian blowfly,

Synthesis of N-substituted γ-methylene γ-lactams

Adhikari, Raju,Jones, Dionne A.,Liepa, Andris J.,Nearn, Roland H.

, p. 882 - 890 (2007/10/03)

N-Substituted cyanoacetamides 1 were condensed with 1,2-diketones 2 under base catalysis to form ?-hydroxy ?-lactams 3. Treatment of 3 with acids gave novel fungicidal ?-methylene ?-lactams 4. The exocyclic double bond of 4b reacted reversibly with 4-toluene sulfinate. CSIRO 2005.

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