Cas 1573120-93-0,((E)-1-ethylidene-1,2,3,4-tetrahydronaphthalen-2-yl)(phenyl)methanone

1573120-93-0

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Basic information

Product Name: ((E)-1-ethylidene-1,2,3,4-tetrahydronaphthalen-2-yl)(phenyl)methanone
Synonyms: ((E)-1-ethylidene-1,2,3,4-tetrahydronaphthalen-2-yl)(phenyl)methanone
CAS NO:1573120-93-0
Molecular Formula:
Molecular Weight: 262.351
EINECS: N/A
Product Categories: N/A
Mol File: 1573120-93-0.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: ((E)-1-ethylidene-1,2,3,4-tetrahydronaphthalen-2-yl)(phenyl)methanone(CAS DataBase Reference)
NIST Chemistry Reference: ((E)-1-ethylidene-1,2,3,4-tetrahydronaphthalen-2-yl)(phenyl)methanone(1573120-93-0)
EPA Substance Registry System: ((E)-1-ethylidene-1,2,3,4-tetrahydronaphthalen-2-yl)(phenyl)methanone(1573120-93-0)

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: 1573120-93-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1573120-93-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,7,3,1,2 and 0 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1573120-93:
(9*1)+(8*5)+(7*7)+(6*3)+(5*1)+(4*2)+(3*0)+(2*9)+(1*3)=150
150 % 10 = 0
So 1573120-93-0 is a valid CAS Registry Number.

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1573120-93-0Relevant articles and documents

Regioselective hydroacylation of 1,3-dienes by cobalt catalysis

Chen, Qing-An,Kim, Daniel K.,Dong, Vy M.

supporting information, p. 3772 - 3775 (2014/04/03)

We describe a cobalt-catalyzed hydroacylation of 1,3-dienes with non-chelating aldehydes. Aromatic aldehydes provide 1,4-addition products as the major isomer, while aliphatic aldehydes favor 1,2-hydroacylation products. The kinetic profile supports an oxidative cyclization mechanism involving a cobaltacycle intermediate that undergoes transformation with high regio- and stereoselectivity.

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