Cas 1421663-84-4,(1E)-N-[1-[[[5-(1,1-dimethylethyl)dimethylsilyl]oxy]-3-[[4-(1,1-dimethylethyl)dimethylsilyl]-oxy]-phenyl]pentyl]-1,3-butadiene-1-sulfonamide

1421663-84-4

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Basic information

Product Name: (1E)-N-[1-[[[5-(1,1-dimethylethyl)dimethylsilyl]oxy]-3-[[4-(1,1-dimethylethyl)dimethylsilyl]-oxy]-phenyl]pentyl]-1,3-butadiene-1-sulfonamide
Synonyms:
CAS NO:1421663-84-4
Molecular Formula:
Molecular Weight: 425.665
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: (1E)-N-[1-[[[5-(1,1-dimethylethyl)dimethylsilyl]oxy]-3-[[4-(1,1-dimethylethyl)dimethylsilyl]-oxy]-phenyl]pentyl]-1,3-butadiene-1-sulfonamide(CAS DataBase Reference)
NIST Chemistry Reference: (1E)-N-[1-[[[5-(1,1-dimethylethyl)dimethylsilyl]oxy]-3-[[4-(1,1-dimethylethyl)dimethylsilyl]-oxy]-phenyl]pentyl]-1,3-butadiene-1-sulfonamide(1421663-84-4)
EPA Substance Registry System: (1E)-N-[1-[[[5-(1,1-dimethylethyl)dimethylsilyl]oxy]-3-[[4-(1,1-dimethylethyl)dimethylsilyl]-oxy]-phenyl]pentyl]-1,3-butadiene-1-sulfonamide(1421663-84-4)

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: 1421663-84-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1421663-84-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,1,6,6 and 3 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1421663-84:
(9*1)+(8*4)+(7*2)+(6*1)+(5*6)+(4*6)+(3*3)+(2*8)+(1*4)=144
144 % 10 = 4
So 1421663-84-4 is a valid CAS Registry Number.

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1421663-84-4Relevant academic research and scientific papers

Further studies toward himandrine via sequential oxidative amidation-intramolecular Diels-Alder reactions

Kasahara, Takahito,Ciufolini, Marco A.

, p. 82 - 90 (2013/03/14)

Exploratory work toward the alkaloid himandrine evaluated the directing ability of a pyrrolidine C-3 substituent in a diastereotopic group elective intramolecular Diels-Alder reaction of a spirodienone obtained by the oxidative amidation of a phenol. The

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