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10565-14-7

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10565-14-7 Usage

General Description

Diethyl (2-nitrophenyl)malonate is a chemical compound with the molecular formula C13H15NO7. It is a yellow, crystalline solid that is used as a reagent in organic synthesis. diethyl (2-nitrophenyl)malonate is often utilized in the preparation of pharmaceuticals, agrochemicals, and other fine chemicals. It is also employed in the production of dyes and pigments. Diethyl (2-nitrophenyl)malonate has potential applications in the field of medicinal chemistry due to its ability to modify organic compounds and create new chemical entities. However, it is important to handle this compound with caution as it may be hazardous if not used properly.

Check Digit Verification of cas no

The CAS Registry Mumber 10565-14-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,5,6 and 5 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 10565-14:
(7*1)+(6*0)+(5*5)+(4*6)+(3*5)+(2*1)+(1*4)=77
77 % 10 = 7
So 10565-14-7 is a valid CAS Registry Number.

10565-14-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name Diethyl (2-nitrophenyl)malonate

1.2 Other means of identification

Product number -
Other names diethyl 2-nitrophenylmalonate

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:10565-14-7 SDS

10565-14-7Relevant articles and documents

Nucleophilic aromatic substitution using Et3SiH/cat. t-Bu-P4 as a system for nucleophile activation

Ueno, Masahiro,Yonemoto, Misato,Hashimoto, Masahiro,Wheatley, Andrew E. H.,Naka, Hiroshi,Kondo, Yoshinori

, p. 2264 - 2266 (2007)

A novel type of deprotonative arylation of nucleophiles was conducted using Et3SiH/cat. t-Bu-P4 and the powerful SNAr reactions of aryl fluorides were accomplished using alcohols and malonates as nucleophiles. The Royal Society of Ch

MULTICYCLIC LONIDAMINE ANALOGS

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Page/Page column 79, (2008/06/13)

The invention provides lonidamine analogs as well as methods of treating cancer and BPH.

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