Cas 94833-89-3,1,2,4-Triazolo[3,4-b][1,3,4]thiadiazol-6(5H)-imine, 5-acetyl-N-[4-(dimethylamino)phenyl]-1,7a-dihydro-1-(phenylmethyl)-

94833-89-3

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Basic information

Product Name: 1,2,4-Triazolo[3,4-b][1,3,4]thiadiazol-6(5H)-imine, 5-acetyl-N-[4-(dimethylamino)phenyl]-1,7a-dihydro-1-(phenylmethyl)-
Synonyms:
CAS NO:94833-89-3
Molecular Formula: C20H22N6OS
Molecular Weight: 394.5
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: 1,2,4-Triazolo[3,4-b][1,3,4]thiadiazol-6(5H)-imine, 5-acetyl-N-[4-(dimethylamino)phenyl]-1,7a-dihydro-1-(phenylmethyl)-(CAS DataBase Reference)
NIST Chemistry Reference: 1,2,4-Triazolo[3,4-b][1,3,4]thiadiazol-6(5H)-imine, 5-acetyl-N-[4-(dimethylamino)phenyl]-1,7a-dihydro-1-(phenylmethyl)-(94833-89-3)
EPA Substance Registry System: 1,2,4-Triazolo[3,4-b][1,3,4]thiadiazol-6(5H)-imine, 5-acetyl-N-[4-(dimethylamino)phenyl]-1,7a-dihydro-1-(phenylmethyl)-(94833-89-3)

Safety Data

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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 94833-89-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 94833-89-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,8,3 and 3 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 94833-89:
(7*9)+(6*4)+(5*8)+(4*3)+(3*3)+(2*8)+(1*9)=173
173 % 10 = 3
So 94833-89-3 is a valid CAS Registry Number.

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94833-89-3Relevant academic research and scientific papers

1,3-vs- 1,5-DIPOLAR REACTIVITY OF 1-PHENYLMETHYL-4N-ACETYLIMINO-1H-1,2,4-TRIAZOLIUM BETAIN TOWARD AROMATIC ISOTHIOCYANATES

Zalupsky, Peter,Martvon, Augustin

, p. 1713 - 1721 (2007/10/02)

The title betain I was found to display both 1,3- and 1,5-dipolar reactivity, depending on reaction conditions.Whereas the reaction with aromatic isothiocyanates in nonpolar solvents produced cycloadducts in concerted manner stepwise addition in dimethylf

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