Cas 862424-27-9,N-[2-(but-3-ynyl)hexa-3,4-dienyl]-4-methyl-N-(prop-2-ynyl)benzenesulfonamide

862424-27-9

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Basic information

Product Name: N-[2-(but-3-ynyl)hexa-3,4-dienyl]-4-methyl-N-(prop-2-ynyl)benzenesulfonamide
Synonyms: N-[2-(but-3-ynyl)hexa-3,4-dienyl]-4-methyl-N-(prop-2-ynyl)benzenesulfonamide
CAS NO:862424-27-9
Molecular Formula:
Molecular Weight: 341.474
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-[2-(but-3-ynyl)hexa-3,4-dienyl]-4-methyl-N-(prop-2-ynyl)benzenesulfonamide(CAS DataBase Reference)
NIST Chemistry Reference: N-[2-(but-3-ynyl)hexa-3,4-dienyl]-4-methyl-N-(prop-2-ynyl)benzenesulfonamide(862424-27-9)
EPA Substance Registry System: N-[2-(but-3-ynyl)hexa-3,4-dienyl]-4-methyl-N-(prop-2-ynyl)benzenesulfonamide(862424-27-9)

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: 862424-27-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 862424-27-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,2,4,2 and 4 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 862424-27:
(8*8)+(7*6)+(6*2)+(5*4)+(4*2)+(3*4)+(2*2)+(1*7)=169
169 % 10 = 9
So 862424-27-9 is a valid CAS Registry Number.

862424-27-9Upstream product

862424-27-9Downstream Products

862424-34-8 4-methyl-N-[(4-methylidene-3-vinylcyclohex-2-enyl)methyl]-N-(prop-2-ynyl)benzenesulfonamide

862424-27-9Relevant academic research and scientific papers

Consecutive Rh(I)-catalyzed Alder-ene/Diels-Alder/Diels-Alder reaction sequence affording rapid entry to polycyclic compounds

Brummond, Kay M.,You, Lingfeng

, p. 6180 - 6185 (2005)

Conversion of acyclic allenynes to polycyclic compounds using consecutive transition metal catalyzed carbon-carbon bond forming reactions in a single chemical operation is described. Reaction of an allenyne with a Rh(I) catalyst affords a cross-conjugated

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