Cas 83605-96-3,7-Hydroxy-6-methyl-5,8-dioxo-2,3,5,8-tetrahydro-1H-pyrrolo[1,2-a]indole-9-carboxylic acid ethyl ester

83605-96-3

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Basic information

Product Name: 7-Hydroxy-6-methyl-5,8-dioxo-2,3,5,8-tetrahydro-1H-pyrrolo[1,2-a]indole-9-carboxylic acid ethyl ester
Synonyms: 7-Hydroxy-6-methyl-5,8-dioxo-2,3,5,8-tetrahydro-1H-pyrrolo[1,2-a]indole-9-carboxylic acid ethyl ester
CAS NO:83605-96-3
Molecular Formula:
Molecular Weight: 289.288
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: 7-Hydroxy-6-methyl-5,8-dioxo-2,3,5,8-tetrahydro-1H-pyrrolo[1,2-a]indole-9-carboxylic acid ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 7-Hydroxy-6-methyl-5,8-dioxo-2,3,5,8-tetrahydro-1H-pyrrolo[1,2-a]indole-9-carboxylic acid ethyl ester(83605-96-3)
EPA Substance Registry System: 7-Hydroxy-6-methyl-5,8-dioxo-2,3,5,8-tetrahydro-1H-pyrrolo[1,2-a]indole-9-carboxylic acid ethyl ester(83605-96-3)

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: 83605-96-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 83605-96-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,6,0 and 5 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 83605-96:
(7*8)+(6*3)+(5*6)+(4*0)+(3*5)+(2*9)+(1*6)=143
143 % 10 = 3
So 83605-96-3 is a valid CAS Registry Number.

83605-96-3Upstream product

35150-22-2 (Z)-ethyl 2-(pyrrolidin-2-ylidene)acetate

83605-96-3Downstream Products

3567-46-2 7-methoxymitosene

83605-96-3Relevant academic research and scientific papers

Expeditious Synthesis of 2,3-Dihydro-1H-pyrroloindoles, Pyrroloindole Quinones, and Related Heterocycles via Nenitzescu-Type Condensation of Quinone Monoketals with Exocyclic Enamino Esters

Coates, Robert M.,MacMann, Patrick A.

, p. 4822 - 4824 (2007/10/02)

Condensation of exocyclic enamino esters with 3-methoxyquinone 4-monoketals gives rise to bicyclic Michael adducts (see Table I) which undergo acid-catalyzed aromatization to 5-methoxypyrroloindole-9-carboxylates suitable for elaboration to mitosenes.

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