Cas 7270-98-6,2-methyl-1-(naphthalen-2-yl)butan-1-one

7270-98-6

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Basic information

Product Name: 2-methyl-1-(naphthalen-2-yl)butan-1-one
Synonyms: 2-methyl-1-(naphthalen-2-yl)butan-1-one
CAS NO:7270-98-6
Molecular Formula:
Molecular Weight: 212.291
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: 2-methyl-1-(naphthalen-2-yl)butan-1-one(CAS DataBase Reference)
NIST Chemistry Reference: 2-methyl-1-(naphthalen-2-yl)butan-1-one(7270-98-6)
EPA Substance Registry System: 2-methyl-1-(naphthalen-2-yl)butan-1-one(7270-98-6)

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: 7270-98-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 7270-98-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,7 and 0 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 7270-98:
(6*7)+(5*2)+(4*7)+(3*0)+(2*9)+(1*8)=106
106 % 10 = 6
So 7270-98-6 is a valid CAS Registry Number.

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7270-98-6Downstream Products

7270-98-6Relevant academic research and scientific papers

Ruthenium-catalyzed tandem-isomerization/asymmetric transfer hydrogenation of allylic alcohols

Slagbrand, Tove,Lundberg, Helena,Adolfsson, Hans

, p. 16102 - 16106 (2014)

A one-pot procedure for the direct conversion of racemic allylic alcohols to enantiomerically enriched saturated alcohols is presented. The tandem-isomerization/ asymmetric transfer hydrogenation process is efficiently catalyzed by [{Ru(p-cymene)Cl2}2] in combination with the a-amino acid hydroxyamide ligand 1, and performed under mild conditions in a mixture of ethanol and THF. The saturated alcohol products are isolated in good to excellent chemical yields and in enantiomeric excess up to 93%.

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