Cas 1111662-46-4,4-{4-n-butyl-1-(3-tolyl)-1H-1,2,3-triazol-5-yl}benzoic acid ethyl ester

1111662-46-4

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Basic information

Product Name: 4-{4-n-butyl-1-(3-tolyl)-1H-1,2,3-triazol-5-yl}benzoic acid ethyl ester
Synonyms: 4-{4-n-butyl-1-(3-tolyl)-1H-1,2,3-triazol-5-yl}benzoic acid ethyl ester
CAS NO:1111662-46-4
Molecular Formula:
Molecular Weight: 363.459
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: 4-{4-n-butyl-1-(3-tolyl)-1H-1,2,3-triazol-5-yl}benzoic acid ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 4-{4-n-butyl-1-(3-tolyl)-1H-1,2,3-triazol-5-yl}benzoic acid ethyl ester(1111662-46-4)
EPA Substance Registry System: 4-{4-n-butyl-1-(3-tolyl)-1H-1,2,3-triazol-5-yl}benzoic acid ethyl ester(1111662-46-4)

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: 1111662-46-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1111662-46-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,1,1,6,6 and 2 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1111662-46:
(9*1)+(8*1)+(7*1)+(6*1)+(5*6)+(4*6)+(3*2)+(2*4)+(1*6)=104
104 % 10 = 4
So 1111662-46-4 is a valid CAS Registry Number.

1111662-46-4Upstream product

1111662-46-4Downstream Products

1111662-46-4Relevant academic research and scientific papers

C-H arylations of 1,2,3-triazoles by reusable heterogeneous palladium catalysts in biomass-derived γ-valerolactone

Tian, Xu,Yang, Fanzhi,Rasina, Dace,Bauer, Michaela,Warratz, Svenja,Ferlin, Francesco,Vaccaro, Luigi,Ackermann, Lutz

supporting information, p. 9777 - 9780 (2016/08/04)

C-H arylations were accomplished with a user-friendly heterogeneous palladium catalyst in the biomass-derived γ-valerolactone (GVL) as an environmentally-benign reaction medium. The user-friendly protocol was characterized by ample substrate scope and hig

Catalytic direct arylations in polyethylene glycol (PEG): Recyclable palladium(O) catalyst for C-H bond cleavages in the presence of air

Ackermann, Lutz,Vicente, Ruben

supporting information; experimental part, p. 4922 - 4925 (2010/01/16)

Two protocols for ruthenium- or palladium-catalyzed direct arylations In user-friendly polyethylene glycol (PEG) were devised, which set the stage for the development of user-friendly paliadium(0)-cataiyzed C-H bond functionalizations In the presence of a

Palladium-catalyzed direct arylations of 1,2,3-triazoles with aryl chlorides using conventional heating

Ackermann, Lutz,Vicente, Ruben,Born, Robert

supporting information; experimental part, p. 741 - 748 (2009/04/10)

Generally applicable, palladium-catalyzed direct arylations of 1,2,3-triazoles with aryl chlorides were accomplished through conventional heating at reaction temperatures of 105-120°C. Thereby, intra- and intermolecular C-H bond functionalizations were achieved with a variety of differently substituted chlorides as electrophiles, bearing numerous valuable functional groups.

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