Cas 1264286-69-2,3-(1,2-O-isopropylidene-3-O-methyl-α-D-xylofuranos-5-ulo-5-yl)-5-(p-chlorobenzoyl)-imidazo[2,1-b]thiazole

1264286-69-2

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Basic information

Product Name: 3-(1,2-O-isopropylidene-3-O-methyl-α-D-xylofuranos-5-ulo-5-yl)-5-(p-chlorobenzoyl)-imidazo[2,1-b]thiazole
Synonyms: 3-(1,2-O-isopropylidene-3-O-methyl-α-D-xylofuranos-5-ulo-5-yl)-5-(p-chlorobenzoyl)-imidazo[2,1-b]thiazole
CAS NO:1264286-69-2
Molecular Formula:
Molecular Weight: 462.911
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: 3-(1,2-O-isopropylidene-3-O-methyl-α-D-xylofuranos-5-ulo-5-yl)-5-(p-chlorobenzoyl)-imidazo[2,1-b]thiazole(CAS DataBase Reference)
NIST Chemistry Reference: 3-(1,2-O-isopropylidene-3-O-methyl-α-D-xylofuranos-5-ulo-5-yl)-5-(p-chlorobenzoyl)-imidazo[2,1-b]thiazole(1264286-69-2)
EPA Substance Registry System: 3-(1,2-O-isopropylidene-3-O-methyl-α-D-xylofuranos-5-ulo-5-yl)-5-(p-chlorobenzoyl)-imidazo[2,1-b]thiazole(1264286-69-2)

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: 1264286-69-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1264286-69-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,4,2,8 and 6 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1264286-69:
(9*1)+(8*2)+(7*6)+(6*4)+(5*2)+(4*8)+(3*6)+(2*6)+(1*9)=172
172 % 10 = 2
So 1264286-69-2 is a valid CAS Registry Number.

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1264286-69-2Relevant academic research and scientific papers

Imidazo[2,1-b]thiazole carbohydrate derivatives: Synthesis and antiviral activity against Junin virus, agent of Argentine hemorrhagic fever

Barradas, José Sebastián,Errea, María Inés,D'Accorso, Norma B.,Sepúlveda, Claudia Soledad,Damonte, Elsa Beatriz

, p. 259 - 264 (2011)

Herein, we describe the syntheses of 3,5-disubstituted imidazo[2,1-b] thiazole. The cyclization step was performed in two different conditions by using either thermal or microwave heating. Comparing the results of both methodologies, we found that the mic

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