Cas 477741-83-6,4H-2,3-Benzodiazepin-4-one, 3,5-dihydro-1-(4-iodophenyl)-7,8-dimethoxy-3-methyl-

477741-83-6

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Basic information

Product Name: 4H-2,3-Benzodiazepin-4-one, 3,5-dihydro-1-(4-iodophenyl)-7,8-dimethoxy-3-methyl-
Synonyms:
CAS NO:477741-83-6
Molecular Formula: C18H17IN2O3
Molecular Weight: 436.249
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: 4H-2,3-Benzodiazepin-4-one, 3,5-dihydro-1-(4-iodophenyl)-7,8-dimethoxy-3-methyl-(CAS DataBase Reference)
NIST Chemistry Reference: 4H-2,3-Benzodiazepin-4-one, 3,5-dihydro-1-(4-iodophenyl)-7,8-dimethoxy-3-methyl-(477741-83-6)
EPA Substance Registry System: 4H-2,3-Benzodiazepin-4-one, 3,5-dihydro-1-(4-iodophenyl)-7,8-dimethoxy-3-methyl-(477741-83-6)

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: 477741-83-6(Hazardous Substances Data)

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477741-83-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 477741-83-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,7,7,4 and 1 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 477741-83:
(8*4)+(7*7)+(6*7)+(5*7)+(4*4)+(3*1)+(2*8)+(1*3)=196
196 % 10 = 6
So 477741-83-6 is a valid CAS Registry Number.

477741-83-6Upstream product

477741-83-6Downstream Products

477741-84-7 7,8-dimethoxy-1-[4-(2-methoxyphenyl)phenyl]-3-methyl-3,5-dihydro-4H-2,3-benzodiazepin-4-one

477741-83-6Relevant academic research and scientific papers

Cyclic nucleotide phosphodiesterase inhibitors, preparation and uses thereof

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Page/Page column 14, (2010/02/08)

The invention concerns novel benzodiazepine derivatives and their uses in the field of therapeutics particularly for treating pathologies involving the activity of a cyclic nucleotide phosphodiesterase. It also concerns methods for preparing them and novel synthesis intermediates. The inventive compounds more particularly correspond to general formula (I):

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