Cas 400741-22-2,Benzoic acid, 2-hydroxy-4-[5-[(tetrahydro-4,6-dioxo-2-thioxo-5(2H)-pyrimidinylidene) methyl]-2-furanyl]-

400741-22-2

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Basic information

Product Name: Benzoic acid, 2-hydroxy-4-[5-[(tetrahydro-4,6-dioxo-2-thioxo-5(2H)-pyrimidinylidene) methyl]-2-furanyl]-
Synonyms:
CAS NO:400741-22-2
Molecular Formula: C16H10N2O6S
Molecular Weight: 358.331
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: Benzoic acid, 2-hydroxy-4-[5-[(tetrahydro-4,6-dioxo-2-thioxo-5(2H)-pyrimidinylidene) methyl]-2-furanyl]-(CAS DataBase Reference)
NIST Chemistry Reference: Benzoic acid, 2-hydroxy-4-[5-[(tetrahydro-4,6-dioxo-2-thioxo-5(2H)-pyrimidinylidene) methyl]-2-furanyl]-(400741-22-2)
EPA Substance Registry System: Benzoic acid, 2-hydroxy-4-[5-[(tetrahydro-4,6-dioxo-2-thioxo-5(2H)-pyrimidinylidene) methyl]-2-furanyl]-(400741-22-2)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 400741-22-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 400741-22-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,0,7,4 and 1 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 400741-22:
(8*4)+(7*0)+(6*0)+(5*7)+(4*4)+(3*1)+(2*2)+(1*2)=92
92 % 10 = 2
So 400741-22-2 is a valid CAS Registry Number.

400741-22-2Upstream product

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400741-22-2Relevant academic research and scientific papers

Exploration of novel thiobarbituric acid-, rhodanine- and thiohydantoin-based HIV-1 integrase inhibitors

Rajamaki, Suvi,Innitzer, Anna,Falciani, Chiara,Tintori, Cristina,Christ, Frauke,Witvrouw, Myriam,Debyser, Zeger,Massa, Silvio,Botta, Maurizio

scheme or table, p. 3615 - 3618 (2010/03/31)

A novel compound inhibiting HIV-1 integrase has been identified by means of virtual screening techniques. A small family of structurally related molecules has been synthesized and biologically evaluated with some of the compounds possessing micromolar act

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