Cas 1287690-40-7,1,13-dimethoxy-N-phenyl-5,9-dipropyl-9,13b-dihydro-5H-quinolino[2,3,4-kl]acridine-13b-carbothioamide

1287690-40-7

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Basic information

Product Name: 1,13-dimethoxy-N-phenyl-5,9-dipropyl-9,13b-dihydro-5H-quinolino[2,3,4-kl]acridine-13b-carbothioamide
Synonyms: 1,13-dimethoxy-N-phenyl-5,9-dipropyl-9,13b-dihydro-5H-quinolino[2,3,4-kl]acridine-13b-carbothioamide
CAS NO:1287690-40-7
Molecular Formula:
Molecular Weight: 549.737
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: 1,13-dimethoxy-N-phenyl-5,9-dipropyl-9,13b-dihydro-5H-quinolino[2,3,4-kl]acridine-13b-carbothioamide(CAS DataBase Reference)
NIST Chemistry Reference: 1,13-dimethoxy-N-phenyl-5,9-dipropyl-9,13b-dihydro-5H-quinolino[2,3,4-kl]acridine-13b-carbothioamide(1287690-40-7)
EPA Substance Registry System: 1,13-dimethoxy-N-phenyl-5,9-dipropyl-9,13b-dihydro-5H-quinolino[2,3,4-kl]acridine-13b-carbothioamide(1287690-40-7)

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: 1287690-40-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1287690-40-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,8,7,6,9 and 0 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1287690-40:
(9*1)+(8*2)+(7*8)+(6*7)+(5*6)+(4*9)+(3*0)+(2*4)+(1*0)=197
197 % 10 = 7
So 1287690-40-7 is a valid CAS Registry Number.

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1287690-40-7Relevant academic research and scientific papers

From cationic to anionic helicenes: New reactivity through umpolung

Conreaux, David,Mehanna, Nathalie,Herse, Christelle,Lacour, Jerome

, p. 2716 - 2722 (2011/06/20)

Using a two-step reduction/metalation procedure, highly stable chiral carbenium ions are transformed into reactive carbanion intermediates. Interesting polar ketone and thioamide products are the results of this umpolung that occurs with complete retentio

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