Cas 183243-53-0,(5S,8R)-5,8-Bis-hydroxymethyl-2-phenyl-tetrahydro-[1,2,4]triazolo[1,2-a]pyridazine-1,3-dione

183243-53-0

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Basic information

Product Name: (5S,8R)-5,8-Bis-hydroxymethyl-2-phenyl-tetrahydro-[1,2,4]triazolo[1,2-a]pyridazine-1,3-dione
Synonyms:
CAS NO:183243-53-0
Molecular Formula:
Molecular Weight: 291.307
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: (5S,8R)-5,8-Bis-hydroxymethyl-2-phenyl-tetrahydro-[1,2,4]triazolo[1,2-a]pyridazine-1,3-dione(CAS DataBase Reference)
NIST Chemistry Reference: (5S,8R)-5,8-Bis-hydroxymethyl-2-phenyl-tetrahydro-[1,2,4]triazolo[1,2-a]pyridazine-1,3-dione(183243-53-0)
EPA Substance Registry System: (5S,8R)-5,8-Bis-hydroxymethyl-2-phenyl-tetrahydro-[1,2,4]triazolo[1,2-a]pyridazine-1,3-dione(183243-53-0)

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: 183243-53-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 183243-53-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,3,2,4 and 3 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 183243-53:
(8*1)+(7*8)+(6*3)+(5*2)+(4*4)+(3*3)+(2*5)+(1*3)=130
130 % 10 = 0
So 183243-53-0 is a valid CAS Registry Number.

183243-53-0Upstream product

10316-53-7 4-phenyl-2,4,6-triazatricyclo[5.2.2.0^2,6]undec-8-ene-3,5-dione

183243-53-0Downstream Products

183243-53-0Relevant academic research and scientific papers

De novo syntheses of enantiopure glycosyl donors of D-/L-azapurpurosamine C type - Enzymatic asymmetrizations

Grabowski, Stefan,Prinzbach, Horst

, p. 7951 - 7954 (1996)

Glycosyl donors of type 1 are synthesized starting from known cycloadducts of 1,3-cyclohexadiene with azo dienophiles and by utilizing biocatalytic asymmetrizations as access to the pure antipodes.

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