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4-(1,3-benzodioxol-5-yl)-2-(5-bromo-2-fluorophenyl)-6-(5-chloro-2-hydroxyphenyl)-1,2,3,6-tetrahydropyrimidin-1-ium is a complex organic compound with a molecular formula of C21H15BrClFN2O3. It is characterized by a tetrahydropyrimidin-1-ium core, which is a heterocyclic compound with four carbon atoms and two nitrogen atoms in a ring structure. The compound features a 1,3-benzodioxole group at the 4-position, which is a benzene ring with two oxygen atoms forming a dioxole ring. At the 2-position, there is a 5-bromo-2-fluorophenyl group, which includes a bromine atom and a fluorine atom attached to a phenyl ring. The 6-position is occupied by a 5-chloro-2-hydroxyphenyl group, which has a chlorine atom and a hydroxyl group on a phenyl ring. 4-(1,3-benzodioxol-5-yl)-2-(5-bromo-2-fluorophenyl)-6-(5-chloro-2-hydroxyphenyl)-1,2,3,6-tetrahydropyrimidin-1-ium is likely to be used in pharmaceutical or chemical research due to its unique structure and potential reactivity.

6776-41-6

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6776-41-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6776-41-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,7,7 and 6 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6776-41:
(6*6)+(5*7)+(4*7)+(3*6)+(2*4)+(1*1)=126
126 % 10 = 6
So 6776-41-6 is a valid CAS Registry Number.

6776-41-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[6-(1,3-benzodioxol-5-yl)-2-(5-bromo-2-fluorophenyl)-1,2,3,4-tetrahydropyrimidin-3-ium-4-yl]-4-chlorophenol

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:6776-41-6 SDS

6776-41-6Downstream Products

6776-41-6Relevant academic research and scientific papers

Reactivity, Selectivity, and Stability in Sulfenic Acid Detection: A Comparative Study of Nucleophilic and Electrophilic Probes

Gupta, Vinayak,Paritala, Hanumantharao,Carroll, Kate S.

, p. 1411 - 1418 (2016/06/09)

The comparative reaction efficiencies of currently used nucleophilic and electrophilic probes toward cysteine sulfenic acid have been thoroughly evaluated in two different settings-(i) a small molecule dipeptide based model and (ii) a recombinant protein model. We further evaluated the stability of corresponding thioether and sulfoxide adducts under reducing conditions which are commonly encountered during proteomic protocols and in cell analysis. Powered by the development of new cyclic and linear C-nucleophiles, the unsurpassed efficiency in the capture of sulfenic acid under competitive conditions is achieved and thus holds great promise as highly potent tools for activity-based sulfenome profiling.

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