Cas 90521-29-2,6-Benzyl-3-(2-chloro-ethyl)-4-oxo-3,4-dihydro-imidazo[5,1-d][1,2,3,5]tetrazine-8-carboxylic acid amide

90521-29-2

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Basic information

Product Name: 6-Benzyl-3-(2-chloro-ethyl)-4-oxo-3,4-dihydro-imidazo[5,1-d][1,2,3,5]tetrazine-8-carboxylic acid amide
Synonyms:
CAS NO:90521-29-2
Molecular Formula:
Molecular Weight: 332.749
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: 6-Benzyl-3-(2-chloro-ethyl)-4-oxo-3,4-dihydro-imidazo[5,1-d][1,2,3,5]tetrazine-8-carboxylic acid amide(CAS DataBase Reference)
NIST Chemistry Reference: 6-Benzyl-3-(2-chloro-ethyl)-4-oxo-3,4-dihydro-imidazo[5,1-d][1,2,3,5]tetrazine-8-carboxylic acid amide(90521-29-2)
EPA Substance Registry System: 6-Benzyl-3-(2-chloro-ethyl)-4-oxo-3,4-dihydro-imidazo[5,1-d][1,2,3,5]tetrazine-8-carboxylic acid amide(90521-29-2)

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: 90521-29-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 90521-29-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,5,2 and 1 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 90521-29:
(7*9)+(6*0)+(5*5)+(4*2)+(3*1)+(2*2)+(1*9)=112
112 % 10 = 2
So 90521-29-2 is a valid CAS Registry Number.

90521-29-2Upstream product

90521-91-8 5-amino-2-benzyl-1⁽³⁾H-imidazole-4-carboxylic acid amide

90521-29-2Downstream Products

90521-29-2Relevant academic research and scientific papers

Antitumor Imidazotetrazines. 14. Synthesis and Antitumor Activity of 6- and 8-Ssubstituted Imidazo-1,2,3,5-tetrazinones and 8-Substituted Pyrazolo-1,2,3,5-tetrazinones

Lunt, Edward,Newton, Christopher G.,Smith, Christopher,Stevens, Graham P.,Stevens, Malcolm F. G.,et al.

, p. 357 - 366 (1987)

The systematic variation of the potent antitumor agent mitozolomide (1) is extended to cover alteration of substituents at position 6 and 8 and to change the imidazo-1,2,3,5-tetrazinone (6) skeleton to the isomeric pyrazolo-1,2,3,5-tetrazino

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