Cas 1449486-48-9,N-(5,5-dimethylhexa-2,3-dien-1-yl)-4-methyl-N-(7-oxohept-2-yn-1-yl)benzenesulfonamide

1449486-48-9

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Basic information

Product Name: N-(5,5-dimethylhexa-2,3-dien-1-yl)-4-methyl-N-(7-oxohept-2-yn-1-yl)benzenesulfonamide
Synonyms: N-(5,5-dimethylhexa-2,3-dien-1-yl)-4-methyl-N-(7-oxohept-2-yn-1-yl)benzenesulfonamide
CAS NO:1449486-48-9
Molecular Formula:
Molecular Weight: 387.543
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: N-(5,5-dimethylhexa-2,3-dien-1-yl)-4-methyl-N-(7-oxohept-2-yn-1-yl)benzenesulfonamide(CAS DataBase Reference)
NIST Chemistry Reference: N-(5,5-dimethylhexa-2,3-dien-1-yl)-4-methyl-N-(7-oxohept-2-yn-1-yl)benzenesulfonamide(1449486-48-9)
EPA Substance Registry System: N-(5,5-dimethylhexa-2,3-dien-1-yl)-4-methyl-N-(7-oxohept-2-yn-1-yl)benzenesulfonamide(1449486-48-9)

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: 1449486-48-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1449486-48-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,9,4,8 and 6 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1449486-48:
(9*1)+(8*4)+(7*4)+(6*9)+(5*4)+(4*8)+(3*6)+(2*4)+(1*8)=209
209 % 10 = 9
So 1449486-48-9 is a valid CAS Registry Number.

1449486-48-9Upstream product

121352-64-5 (Z)-7-((tert-butyldimethylsilyl)oxy)hept-2-yne-1-ol

1449486-48-9Downstream Products

1449486-48-9Relevant academic research and scientific papers

Construction of tricyclic pyran derivatives through intramolecular [2+2+2] cycloaddition of allenynes with tethered aldehydes

Oonishi, Yoshihiro,Kitano, Yoshitaka,Sato, Yoshihiro

supporting information, p. 7713 - 7718 (2013/08/23)

Rh(I)-catalyzed intramolecular [2+2+2] cycloaddition of allenynes with tethered aldehydes was investigated. The cyclizations proceeded smoothly under mild conditions to give various tricyclic compounds containing a pyran ring in good to high yields in a stereoselective manner.

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