Cas 1439599-37-7,(E)-1-benzyl-3-(3,7-dimethylocta-2,6-dien-1-yl)-3-hydroxy-5-methylindolin-2-one

1439599-37-7

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Basic information

Product Name: (E)-1-benzyl-3-(3,7-dimethylocta-2,6-dien-1-yl)-3-hydroxy-5-methylindolin-2-one
Synonyms: (E)-1-benzyl-3-(3,7-dimethylocta-2,6-dien-1-yl)-3-hydroxy-5-methylindolin-2-one
CAS NO:1439599-37-7
Molecular Formula:
Molecular Weight: 389.538
EINECS: N/A
Product Categories: N/A
Mol File: 1439599-37-7.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-benzyl-3-(3,7-dimethylocta-2,6-dien-1-yl)-3-hydroxy-5-methylindolin-2-one(CAS DataBase Reference)
NIST Chemistry Reference: (E)-1-benzyl-3-(3,7-dimethylocta-2,6-dien-1-yl)-3-hydroxy-5-methylindolin-2-one(1439599-37-7)
EPA Substance Registry System: (E)-1-benzyl-3-(3,7-dimethylocta-2,6-dien-1-yl)-3-hydroxy-5-methylindolin-2-one(1439599-37-7)

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: 1439599-37-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1439599-37-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,3,9,5,9 and 9 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1439599-37:
(9*1)+(8*4)+(7*3)+(6*9)+(5*5)+(4*9)+(3*9)+(2*3)+(1*7)=217
217 % 10 = 7
So 1439599-37-7 is a valid CAS Registry Number.

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1439599-37-7Relevant articles and documents

Regioselective ruthenium catalyzed hydrohydroxyalkylation of dienes with 3-hydroxy-2-oxindoles: Prenylation, geranylation, and beyond

Chen, Te-Yu,Krische, Michael J.

, p. 2994 - 2997 (2013/07/26)

The direct conversion of secondary to tertiary alcohols via ruthenium(0) catalyzed C-C coupling of substituted 3-hydroxy-2-oxindoles with various dienes is described. Coupling occurs in a completely regioselective manner in the absence of stoichiometric b

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