Cas 75390-05-5,5-Hydroxy-1-methyl-2-(1'-oxo-5',5'-dimethyl-3'-hydroxy-2'-cyclohexen-2-yl-methyl)-indol-3-carbonsaeureethylester

75390-05-5

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Basic information

Product Name: 5-Hydroxy-1-methyl-2-(1'-oxo-5',5'-dimethyl-3'-hydroxy-2'-cyclohexen-2-yl-methyl)-indol-3-carbonsaeureethylester
Synonyms: 5-Hydroxy-1-methyl-2-(1'-oxo-5',5'-dimethyl-3'-hydroxy-2'-cyclohexen-2-yl-methyl)-indol-3-carbonsaeureethylester
CAS NO:75390-05-5
Molecular Formula:
Molecular Weight: 371.433
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: 5-Hydroxy-1-methyl-2-(1'-oxo-5',5'-dimethyl-3'-hydroxy-2'-cyclohexen-2-yl-methyl)-indol-3-carbonsaeureethylester(CAS DataBase Reference)
NIST Chemistry Reference: 5-Hydroxy-1-methyl-2-(1'-oxo-5',5'-dimethyl-3'-hydroxy-2'-cyclohexen-2-yl-methyl)-indol-3-carbonsaeureethylester(75390-05-5)
EPA Substance Registry System: 5-Hydroxy-1-methyl-2-(1'-oxo-5',5'-dimethyl-3'-hydroxy-2'-cyclohexen-2-yl-methyl)-indol-3-carbonsaeureethylester(75390-05-5)

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: 75390-05-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 75390-05-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,3,9 and 0 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 75390-05:
(7*7)+(6*5)+(5*3)+(4*9)+(3*0)+(2*0)+(1*5)=135
135 % 10 = 5
So 75390-05-5 is a valid CAS Registry Number.

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75390-05-5Downstream Products

75390-05-5Relevant academic research and scientific papers

Synthesis of Substituted Indole Derivatives II: The Reactivity of a Cyclic Quinonecarbinolamine

Kucklaender, Uwe,Edoho, Edoho J.

, p. 697 - 701 (1980)

The cyclic quinonecarbinolamine 1 reacts with basic nucleophiles to yield the indolemethylene derivatives 3 via an enol tautomer of 1.

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