Cas 1198575-54-0,(1E)-1-{2-[(1E)-1-benzylidenepropyl]phenyl}ethanone oxime

1198575-54-0

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Basic information

Product Name: (1E)-1-{2-[(1E)-1-benzylidenepropyl]phenyl}ethanone oxime
Synonyms: (1E)-1-{2-[(1E)-1-benzylidenepropyl]phenyl}ethanone oxime
CAS NO:1198575-54-0
Molecular Formula:
Molecular Weight: 265.355
EINECS: N/A
Product Categories: N/A
Mol File: 1198575-54-0.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: (1E)-1-{2-[(1E)-1-benzylidenepropyl]phenyl}ethanone oxime(CAS DataBase Reference)
NIST Chemistry Reference: (1E)-1-{2-[(1E)-1-benzylidenepropyl]phenyl}ethanone oxime(1198575-54-0)
EPA Substance Registry System: (1E)-1-{2-[(1E)-1-benzylidenepropyl]phenyl}ethanone oxime(1198575-54-0)

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: 1198575-54-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1198575-54-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,8,5,7 and 5 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1198575-54:
(9*1)+(8*1)+(7*9)+(6*8)+(5*5)+(4*7)+(3*5)+(2*5)+(1*4)=210
210 % 10 = 0
So 1198575-54-0 is a valid CAS Registry Number.

1198575-54-0Upstream product

1198575-54-0Downstream Products

1198575-52-8 1-methyl-3-ethyl-4-phenylisoquinoline

1198575-54-0Relevant articles and documents

Easy access to isoquinolines and tetrahydroquinolines from ketoximes and alkynes via rhodium-catalyzed C-H bond activation

Parthasarathy, Kanniyappan,Cheng, Chien-Hong

, p. 9359 - 9364 (2009)

(Chemical Equation Presented) Described herein is a convenient and highly regioselective synthesis of substituted isoquinoline derivatives from various aromatic ketoximes and alkynes via a one-pot, rhodium-catalyzed C-H bond activation. In addition, tetra

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