Cas 872971-64-7,Pyrrolo[2,3-c]azepin-8(1H)-one, 4-(2-amino-4,5-dihydro-5-oxo-1H-imidazol-4-yl)-6,7-dihydro-

872971-64-7

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Basic information

Product Name: Pyrrolo[2,3-c]azepin-8(1H)-one, 4-(2-amino-4,5-dihydro-5-oxo-1H-imidazol-4-yl)-6,7-dihydro-
Synonyms:
CAS NO:872971-64-7
Molecular Formula: C11H11N5O2
Molecular Weight:
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: Pyrrolo[2,3-c]azepin-8(1H)-one, 4-(2-amino-4,5-dihydro-5-oxo-1H-imidazol-4-yl)-6,7-dihydro-(CAS DataBase Reference)
NIST Chemistry Reference: Pyrrolo[2,3-c]azepin-8(1H)-one, 4-(2-amino-4,5-dihydro-5-oxo-1H-imidazol-4-yl)-6,7-dihydro-(872971-64-7)
EPA Substance Registry System: Pyrrolo[2,3-c]azepin-8(1H)-one, 4-(2-amino-4,5-dihydro-5-oxo-1H-imidazol-4-yl)-6,7-dihydro-(872971-64-7)

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: 872971-64-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 872971-64-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,2,9,7 and 1 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 872971-64:
(8*8)+(7*7)+(6*2)+(5*9)+(4*7)+(3*1)+(2*6)+(1*4)=217
217 % 10 = 7
So 872971-64-7 is a valid CAS Registry Number.

872971-64-7Upstream product

872971-64-7Downstream Products

125118-55-0 (Z)-debromohymenialdisine

872971-64-7Relevant academic research and scientific papers

A new glycociamidine ring precursor: Syntheses of (Z)-hymenialdisine, (Z)-2-debromohymenialdisine, and (±)-endo-2-debromohymenialdisine

Papeo, Gianluca,Posteri, Helena,Borghi, Daniela,Varasi, Mario

, p. 5641 - 5644 (2005)

(Chemical Equation Presented) The synthesis of the C11H 5 marine sponge alkaloids, (Z)-hymenialdisine and (Z)-2-debromohymenialdisine, is described. A key step was the condensation between aldisine or its monobromo derivative and a n

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