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16034-46-1

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16034-46-1 Usage

Chemical Properties

White to yellow solid

Check Digit Verification of cas no

The CAS Registry Mumber 16034-46-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,0,3 and 4 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 16034-46:
(7*1)+(6*6)+(5*0)+(4*3)+(3*4)+(2*4)+(1*6)=81
81 % 10 = 1
So 16034-46-1 is a valid CAS Registry Number.
InChI:InChI=1/C5H6N2O2/c1-7-4(5(8)9)2-3-6-7/h2-3H,1H3,(H,8,9)

16034-46-1 Well-known Company Product Price

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  • Alfa Aesar

  • (H32874)  1-Methyl-1H-pyrazole-5-carboxylic acid, 97%   

  • 16034-46-1

  • 250mg

  • 584.0CNY

  • Detail
  • Alfa Aesar

  • (H32874)  1-Methyl-1H-pyrazole-5-carboxylic acid, 97%   

  • 16034-46-1

  • 1g

  • 1437.0CNY

  • Detail
  • Aldrich

  • (722138)  1-Methyl-1H-pyrazole-5-carboxylicacid  97%

  • 16034-46-1

  • 722138-1G

  • 1,329.12CNY

  • Detail

16034-46-1Downstream Products

16034-46-1Relevant articles and documents

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Balterham,Bigum

, p. 431 (1969)

-

Room Temperature Carbonylation of (Hetero) Aryl Pentafluorobenzenesulfonates and Triflates using Palladium-Cobalt Bimetallic Catalyst: Dual Role of Cobalt Carbonyl

Joseph, Jayan T.,Sajith, Ayyiliath M.,Ningegowda, Revanna C.,Shashikanth, Sheena

supporting information, p. 419 - 425 (2017/02/10)

An efficient method for the carbonylation of (hetero) aryl pentafluorobenzenesulfonates and triflates under exceptionally mild conditions using palladium/dicobalt octacarbonyl [Pd/Co2(CO)8] has been developed. Besides acting as carbon monoxide (CO) source, Co2(CO)8enhances the reaction rate by accelerating the CO insertion through an in situ generated bimetallic palladium cobalt tetracarbonyl [Pd-Co(CO)4] complex. Under the optimized reaction condition, carbonylation of a wide range of activated and deactivated, as well as sterically hindered and heteroaromatic, substrates proceeded efficiently at room temperature. The high chemoselectivity and improved synthesis of biologically relevant Isoguvacine and Lazabemide intermediates highlights its scope as a valuable synthetic method. The generality of this protocol was further extended to other electrophiles (bromides, chlorides and tosylates). (Figure presented.).

Discovery and Optimization of Selective Nav1.8 Modulator Series That Demonstrate Efficacy in Preclinical Models of Pain

Bagal, Sharan K.,Bungay, Peter J.,Denton, Stephen M.,Gibson, Karl R.,Glossop, Melanie S.,Hay, Tanya L.,Kemp, Mark I.,Lane, Charlotte A. L.,Lewis, Mark L.,Maw, Graham N.,Million, William A.,Payne, C. Elizabeth,Poinsard, Cedric,Rawson, David J.,Stammen, Blanda L.,Stevens, Edward B.,Thompson, Lisa R.

, p. 650 - 654 (2015/06/30)

Voltage-gated sodium channels, in particular Nav1.8, can be targeted for the treatment of neuropathic and inflammatory pain. Herein, we described the optimization of Nav1.8 modulator series to deliver subtype selective, state, and use-dependent chemical matter that is efficacious in preclinical models of neuropathic and inflammatory pain. (Chemical Presented).

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