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PROPANEDIOIC ACID, 2-[2-NITRO-1-(4-NITROPHENYL)ETHYL]-, 1,3-DIMETHYL ESTER is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

100796-42-7

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100796-42-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 100796-42-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,7,9 and 6 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 100796-42:
(8*1)+(7*0)+(6*0)+(5*7)+(4*9)+(3*6)+(2*4)+(1*2)=107
107 % 10 = 7
So 100796-42-7 is a valid CAS Registry Number.
InChI:InChI=1/C13H14N2O8/c1-22-12(16)11(13(17)23-2)10(7-14(18)19)8-3-5-9(6-4-8)15(20)21/h3-6,10-11H,7H2,1-2H3

100796-42-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name dimethyl 2-[2-nitro-1-(4-nitrophenyl)ethyl]malonate

1.2 Other means of identification

Product number -
Other names [2-Nitro-1-(4-nitro-phenyl)-aethyl]-malonsaeure-dimethylester

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:100796-42-7 SDS

100796-42-7Relevant academic research and scientific papers

Divergent Reactivity of Nitrocyclopropanes with Huisgen Zwitterions and Facile Syntheses of 3-Alkoxy Pyrazolines and Pyrazoles

Yang, Changjiang,Liu, Wei,He, Zijian,He, Zhengjie

supporting information, p. 4936 - 4939 (2016/10/18)

A novel annulation reaction of trans-2-substituted-3-nitrocyclopropane-1,1-carboxylates with in situ generated Huisgen zwitterions is reported, providing facile synthesis of 3-alkoxy pyrazolines in good yields and high diastereoselectivities. This reactio

Iodine-promoted synthesis of 3-arylindolizine-1-carboxylates from 2-(2-nitro-1-arylethyl)malonates and pyridine

Li, Yun,Zhou, Zhengquan,Ye, Weijian,Liu, Juanjuan,Yao, Juan,Wang, Cunde

, p. 526 - 530 (2013/10/22)

An efficient and straightforward one-pot synthetic protocol has been developed for the synthesis of 3-arylindolizine- 1-carboxylates via 1,3-dipolar annulation of 2-(2-nitro-1-arylethyl)malonates with pyridine and subsequent aromatisation in the presence of molecular iodine. The structure of methyl 3-(4-methoxyphenyl)indolizine-1-carboxylate (2a) and methyl 3-iodo-2-(4- nitrophenyl)indolizine-1-carboxylate (2f) was further confirmed by X-ray single crystal analysis. Website

Highly enantioselective Michael addition of malonates to nitroolefins catalyzed by chiral bifunctional tertiary amine-thioureas based on saccharides

Li, Xiao-Juan,Liu, Kun,Ma, Hai,Nie, Jing,Ma, Jun-An

scheme or table, p. 3242 - 3246 (2009/06/25)

A series of saccharide-derived bifunctional tertiary amine-thioureas for the asymmetric Michael addition reaction have been designed and synthesized. The addition products between malonates and various nitroolefins were obtained in high yields (up to 99%)

1,5,7-Triazabicyclo[4.4.0]dec-5-ene (TBD) catalyzed Michael reactions

Ye, Weiping,Xu, Junye,Tan, Chin-Tong,Tan, Choon-Hong

, p. 6875 - 6878 (2007/10/03)

1,5,7-Triazabicyclo[4.4.0]dec-5-ene (TBD), a bicyclic guanidine base, has been found to be an excellent catalyst for Michael and Michael-type reactions. A wide variety of Michael donors and acceptors can participate in these reactions using 10-20 mol % of

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