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(2Z)-3-chloro-3-(4-nitrophenyl)prop-2-enal is a chemical compound with the molecular formula C9H6ClNO3. It is an organic molecule characterized by a conjugated enal structure, featuring a double bond between the second and third carbon atoms. The compound contains a chloro group at the third carbon and a 4-nitrophenyl group attached to the same carbon. The 4-nitrophenyl group has a nitro group (-NO2) at the para position relative to the phenyl ring. (2Z)-3-chloro-3-(4-nitrophenyl)prop-2-enal is known for its reactivity and can be used in the synthesis of various pharmaceuticals and other organic compounds due to its unique functional groups. It is important to handle this chemical with care, as it may have potential health and environmental impacts due to the presence of the nitro group.

2888-10-0

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2888-10-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2888-10-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,8 and 8 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2888-10:
(6*2)+(5*8)+(4*8)+(3*8)+(2*1)+(1*0)=110
110 % 10 = 0
So 2888-10-0 is a valid CAS Registry Number.

2888-10-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (Z)-3-chloro-3-(4-nitrophenyl)prop-2-enal

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

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More Details:2888-10-0 SDS

2888-10-0Relevant academic research and scientific papers

Novel benzenesulfonamide-bearing pyrazoles and 1,2,4-thiadiazoles as selective carbonic anhydrase inhibitors

Kumar, Rajiv,Kumar, Amit,Ram, Sita,Angeli, Andrea,Bonardi, Alessandro,Nocentini, Alessio,Gratteri, Paola,Supuran, Claudiu T.,Sharma, Pawan K.

, (2021/10/05)

Two series comprising 20 novel benzenesulfonamides bearing thioureido-linked pyrazole 8 and amino-1,2,4-thiadiazole 10 were synthesized and assayed as human carbonic anhydrase (hCA) inhibitors against isoforms I and II as well as the tumor-associated isof

A general and efficient approach to 2H-indazoles and 1H-pyrazoles through copper-catalyzed intramolecular N-N bond formation under mild conditions

Hu, Jiantao,Cheng, Yongfeng,Yang, Yiqing,Rao, Yu

supporting information; experimental part, p. 10133 - 10135 (2011/10/09)

A new efficient copper-catalyzed intramolecular amination reaction has been developed to readily synthesise a wide variety of multi-substituted 2H-indazole and 1H-pyrazole derivatives from easily accessible starting materials under mild conditions. A highly selective ligand for estrogen receptor β was prepared in three steps by employing this method. The Royal Society of Chemistry 2011.

Synthesis of selenophene analogues of the tacrine series: Comparison of classical route and microwave irradiation

Thomae, David,Kirsch, Gilbert,Seck, Pierre

scheme or table, p. 1600 - 1606 (2009/04/03)

New 3-amino-2-selenophenecarbonitriles condensed with cyclanones to afford, in one step, analogues of Tacrine. A comparison between classical heating and microwave irradiation for the Friedlaender condensation is presented. Georg Thieme Verlag Stuttgart.

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