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N-naphthalen-1-yl-2-phenylhydrazinecarbothioamide is a complex organic chemical compound with the molecular formula C17H14N2S. It is characterized by a naphthalene ring (a fused pair of benzene rings) connected to a phenyl ring (a single benzene ring) through a hydrazinecarbothioamide group. N-naphthalen-1-yl-2-phenylhydrazinecarbothioamide is known for its potential applications in the synthesis of various pharmaceuticals and chemical intermediates, particularly in the area of medicinal chemistry. Its structure provides a unique set of properties that can be exploited in the design of new drugs and other chemical products. The compound's specific reactivity and interaction with other molecules make it a valuable component in the development of novel chemical entities.

2078-93-5

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2078-93-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2078-93-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,7 and 8 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2078-93:
(6*2)+(5*0)+(4*7)+(3*8)+(2*9)+(1*3)=85
85 % 10 = 5
So 2078-93-5 is a valid CAS Registry Number.

2078-93-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-anilino-3-naphthalen-1-ylthiourea

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

More Details:2078-93-5 SDS

2078-93-5Relevant academic research and scientific papers

Bioorthogonal Click and Release Reaction of Iminosydnones with Cycloalkynes

Bernard, Sabrina,Audisio, Davide,Riomet, Margaux,Bregant, Sarah,Sallustrau, Antoine,Plougastel, Lucie,Decuypere, Elodie,Gabillet, Sandra,Kumar, Ramar Arun,Elyian, Jijy,Trinh, Minh Nguyet,Koniev, Oleksandr,Wagner, Alain,Kolodych, Sergii,Taran, Frédéric

supporting information, p. 15612 - 15616 (2017/12/02)

We report the discovery of a new bioorthogonal click-and-release reaction involving iminosydnones and strained alkynes. This transformation leads to two products resulting from the ligation and fragmentation of iminosydnones under physiological conditions. Optimized iminosydnones were successfully used to design innovative cleavable linkers for protein modification, thus opening up new areas in the fields of drug release and target-fishing applications. This click-and-release technology offers the possibility of exchanging tags on proteins for functionalized cyclooctynes under mild and bioorthogonal conditions.

Colorimetric Naphthalene-Based Thiosemicarbazide Anion Chemosensors with an Internal Charge Transfer Mechanism

Farrugia, Kristina N.,Makuc, Damjan,Podborska, Agnieszka,Szaci?owski, Konrad,Plavec, Janez,Magri, David C.

supporting information, p. 4415 - 4422 (2016/09/14)

A series of thiosemicarbazide anion chemosensors substituted with naphthalene and 4-nitrophenyl or phenyl units were synthesized. The molecules were characterized by using1H,13C DEPT and15N NMR spectroscopy. The anion bind

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