Cas 1585206-47-8,tert-butyl (Z)-3-(5-fluoro-2-oxoindolin-3-ylidene)-4-oxo-4-phenylbutanoate

1585206-47-8

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Basic information

Product Name: tert-butyl (Z)-3-(5-fluoro-2-oxoindolin-3-ylidene)-4-oxo-4-phenylbutanoate
Synonyms: tert-butyl (Z)-3-(5-fluoro-2-oxoindolin-3-ylidene)-4-oxo-4-phenylbutanoate
CAS NO:1585206-47-8
Molecular Formula:
Molecular Weight: 381.404
EINECS: N/A
Product Categories: N/A
Mol File: 1585206-47-8.mol
Article Data: 1

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: tert-butyl (Z)-3-(5-fluoro-2-oxoindolin-3-ylidene)-4-oxo-4-phenylbutanoate(CAS DataBase Reference)
NIST Chemistry Reference: tert-butyl (Z)-3-(5-fluoro-2-oxoindolin-3-ylidene)-4-oxo-4-phenylbutanoate(1585206-47-8)
EPA Substance Registry System: tert-butyl (Z)-3-(5-fluoro-2-oxoindolin-3-ylidene)-4-oxo-4-phenylbutanoate(1585206-47-8)

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: 1585206-47-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1585206-47-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,8,5,2,0 and 6 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1585206-47:
(9*1)+(8*5)+(7*8)+(6*5)+(5*2)+(4*0)+(3*6)+(2*4)+(1*7)=178
178 % 10 = 8
So 1585206-47-8 is a valid CAS Registry Number.

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1585206-47-8Relevant articles and documents

Synthesis of complex dispirocyclopentanebisoxindoles via cycloaddition reactions of 4-dimethylamino-1-alkoxycarbonylmethylpyridinium bromides with 2-oxoindolin-3-ylidene derivatives

Lu, Li-Juan,Fu, Qin,Sun, Jing,Yan, Chao-Guo

, p. 2537 - 2545 (2014/04/03)

The cycloaddition reactions of 4-dimethylamino-1- alkoxycarbonylmethylpyridinium bromides with various 2-oxoindolin-3-ylidene derivatives in ethanol in the presence of triethylamine afforded the unprecedented dispirocyclopentanebisoxindole derivatives in

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