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N-[(2Z)-4-fluoro-3-prop-2-en-1-yl-1,3-benzothiazol-2(3H)-ylidene]-5-nitrofuran-2-carboxamidato is a complex organic chemical compound with the molecular formula C16H8FN3O5S. It is characterized by a 1,3-benzothiazole core, which is substituted with a 4-fluoro-3-prop-2-en-1-yl group and a 5-nitrofuran-2-carboxamidato group. N-[(2Z)-4-fluoro-3-prop-2-en-1-yl-1,3-benzothiazol-2(3H)-ylidene]-5-nitrofuran-2-carboxamidato is known for its potential applications in the field of pharmaceuticals, particularly as an antimicrobial agent. Its structure features a conjugated system that contributes to its biological activity, and the presence of a nitro group enhances its reactivity and potential therapeutic effects. The compound's specific properties and applications are subject to ongoing research, as its complex structure offers a range of possibilities for drug development and other chemical uses.

6281-65-8

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6281-65-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6281-65-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,8 and 1 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6281-65:
(6*6)+(5*2)+(4*8)+(3*1)+(2*6)+(1*5)=98
98 % 10 = 8
So 6281-65-8 is a valid CAS Registry Number.

6281-65-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N'-bis(1,1,3,3-tetramethylbutyl)-Sulfamide

1.2 Other means of identification

Product number -
Other names 2,2'-Sulfamidobis(2,4,4-trimethylpentane)

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:6281-65-8 SDS

6281-65-8Relevant academic research and scientific papers

Thiadiaziridine 1,1-Dioxides: Synthesis and Chemistry

Timberlake, Jack W.,Alender, Jeff,Garner, Archie W.,Hodges, Melvin L.,Oezmeral, Cenan,et al.

, p. 2082 - 2089 (2007/10/02)

The synthesis and chemical reactions of a series of thiadiaziridine 1,1-dioxides (2) are described.The thermal stability is highly dependent on the R group and in one case (R = tert-octyl) is postulated that the thermolysis initially produces a diradical intermediate which can be trapped or further fragments to give a nitrene.A temperature-dependent NMR study on the coalescence of the diastereotopic α-methyl protons of 2b gives a ΔG = 20 kcal*mol-1.

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