Cas 615562-57-7,<i>N</i>-but-2-ynyl-4-methyl-<i>N</i>-[6-(tetrahydro-pyran-2-yloxy)-hex-2-ynyl]-benzenesulfonamide

615562-57-7

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Basic information

Product Name: N-but-2-ynyl-4-methyl-N-[6-(tetrahydro-pyran-2-yloxy)-hex-2-ynyl]-benzenesulfonamide
Synonyms: N-but-2-ynyl-4-methyl-N-[6-(tetrahydro-pyran-2-yloxy)-hex-2-ynyl]-benzenesulfonamide
CAS NO:615562-57-7
Molecular Formula:
Molecular Weight: 403.543
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-but-2-ynyl-4-methyl-N-[6-(tetrahydro-pyran-2-yloxy)-hex-2-ynyl]-benzenesulfonamide(CAS DataBase Reference)
NIST Chemistry Reference: N-but-2-ynyl-4-methyl-N-[6-(tetrahydro-pyran-2-yloxy)-hex-2-ynyl]-benzenesulfonamide(615562-57-7)
EPA Substance Registry System: N-but-2-ynyl-4-methyl-N-[6-(tetrahydro-pyran-2-yloxy)-hex-2-ynyl]-benzenesulfonamide(615562-57-7)

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: 615562-57-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 615562-57-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,1,5,5,6 and 2 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 615562-57:
(8*6)+(7*1)+(6*5)+(5*5)+(4*6)+(3*2)+(2*5)+(1*7)=157
157 % 10 = 7
So 615562-57-7 is a valid CAS Registry Number.

615562-57-7Upstream product

615562-57-7Downstream Products

615562-39-5 N-but-2-ynyl-N-(6-hydroxy-hex-2-ynyl)-4-methyl-benzenesulfonamide

615562-57-7Relevant academic research and scientific papers

A mechanistic dichotomy in ruthenium-catalyzed propargyl alcohol reactivity: A novel hydrative diyne cyclization

Trost, Barry M.,Rudd, Michael T.

, p. 11516 - 11517 (2003)

The cycloisomerization of diyne-ols catalyzed by [CpRu(CH3CN)3]PF6 to 2-vinyl-1-acylcycloalkenes proceeds via a ruthenacyclopentadiene involving initial ionization of the tertiary or secondary alcohol, followed by readditi

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