Cas 705962-76-1,4-methyl-N-[(2E)-2-methylpenta-2,4-dienyl]-N-[(2E)-penta-2,4-dienyl]benzenesulfonamide

705962-76-1

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Basic information

Product Name: 4-methyl-N-[(2E)-2-methylpenta-2,4-dienyl]-N-[(2E)-penta-2,4-dienyl]benzenesulfonamide
Synonyms: 4-methyl-N-[(2E)-2-methylpenta-2,4-dienyl]-N-[(2E)-penta-2,4-dienyl]benzenesulfonamide
CAS NO:705962-76-1
Molecular Formula:
Molecular Weight: 317.452
EINECS: N/A
Product Categories: N/A
Mol File: 705962-76-1.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: 4-methyl-N-[(2E)-2-methylpenta-2,4-dienyl]-N-[(2E)-penta-2,4-dienyl]benzenesulfonamide(CAS DataBase Reference)
NIST Chemistry Reference: 4-methyl-N-[(2E)-2-methylpenta-2,4-dienyl]-N-[(2E)-penta-2,4-dienyl]benzenesulfonamide(705962-76-1)
EPA Substance Registry System: 4-methyl-N-[(2E)-2-methylpenta-2,4-dienyl]-N-[(2E)-penta-2,4-dienyl]benzenesulfonamide(705962-76-1)

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: 705962-76-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 705962-76-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,0,5,9,6 and 2 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 705962-76:
(8*7)+(7*0)+(6*5)+(5*9)+(4*6)+(3*2)+(2*7)+(1*6)=181
181 % 10 = 1
So 705962-76-1 is a valid CAS Registry Number.

705962-76-1Upstream product

705962-76-1Downstream Products

705962-78-3 methyl (2S)-2-{(3R,4R)-4-methyl-1-[(1E)-phenylprop-1-enyl]-(4-methylbenzenesulfonyl)pyrrolidin-3-yl}but-3-enoate

705962-76-1Relevant articles and documents

Highly Enantioselective Catalytic Carbon Dioxide Incorporation Reaction: Nickel-Catalyzed Asymmetric Carboxylative Cyclization of Bis-1,3-dienes

Takimoto, Masanori,Nakamura, Yoichi,Kimura, Kaoru,Mori, Miwako

, p. 5956 - 5957 (2004)

A method for nickel-catalyzed asymmetric carbon dioxide (CO2) incorporation via carbon-carbon bond formation was developed. In the presence of a catalytic amount of Ni(acac)2 and MeO-MOP, various bis-1,3-dienes reacted with CO2

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