Cas 1386262-26-5,(Z)-1-ethyl-5'-(4-fluorobenzylidene)-4,6-dimethoxy-5'H-spiro-[indoline-3,2'-thiophen]-2-one

1386262-26-5

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Basic information

Product Name: (Z)-1-ethyl-5'-(4-fluorobenzylidene)-4,6-dimethoxy-5'H-spiro-[indoline-3,2'-thiophen]-2-one
Synonyms: (Z)-1-ethyl-5'-(4-fluorobenzylidene)-4,6-dimethoxy-5'H-spiro-[indoline-3,2'-thiophen]-2-one
CAS NO:1386262-26-5
Molecular Formula:
Molecular Weight: 397.47
EINECS: N/A
Product Categories: N/A
Mol File: 1386262-26-5.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: (Z)-1-ethyl-5'-(4-fluorobenzylidene)-4,6-dimethoxy-5'H-spiro-[indoline-3,2'-thiophen]-2-one(CAS DataBase Reference)
NIST Chemistry Reference: (Z)-1-ethyl-5'-(4-fluorobenzylidene)-4,6-dimethoxy-5'H-spiro-[indoline-3,2'-thiophen]-2-one(1386262-26-5)
EPA Substance Registry System: (Z)-1-ethyl-5'-(4-fluorobenzylidene)-4,6-dimethoxy-5'H-spiro-[indoline-3,2'-thiophen]-2-one(1386262-26-5)

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: 1386262-26-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1386262-26-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,8,6,2,6 and 2 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1386262-26:
(9*1)+(8*3)+(7*8)+(6*6)+(5*2)+(4*6)+(3*2)+(2*2)+(1*6)=175
175 % 10 = 5
So 1386262-26-5 is a valid CAS Registry Number.

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1386262-26-5Relevant articles and documents

Cu(II)-promoted transformations of α-thienylcarbinols into spirothienooxindoles: Regioselective halogenation of dienyl sulfethers containing electron-rich aryl rings

Yin, Biaolin,Huang, Li,Zhang, Xiaoyu,Ji, Fanghua,Jiang, Huanfeng

, p. 6365 - 6370 (2012/09/22)

Under the promotion of Cu(II) salts, the α-thienylcarbinols with an N-phenyl carbonyl group at the other α-position are converted into three different ranges of spirothienooxindoles involving dearomatizing Friedel-Crafts reaction. In addition, the unprece

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