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tert-butyl 1-(4-fluorophenyl)hydrazinecarboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1075749-75-5

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1075749-75-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1075749-75-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,7,5,7,4 and 9 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1075749-75:
(9*1)+(8*0)+(7*7)+(6*5)+(5*7)+(4*4)+(3*9)+(2*7)+(1*5)=185
185 % 10 = 5
So 1075749-75-5 is a valid CAS Registry Number.

1075749-75-5Relevant academic research and scientific papers

Continuous flow synthesis of arylhydrazines: via nickel/photoredox coupling of tert -butyl carbazate with aryl halides

Mata, Alejandro,Tran, Duc N.,Weigl, Ulrich,Williams, Jason D.,Kappe, C. Oliver

supporting information, p. 14621 - 14624 (2020/12/02)

Nickel/photoredox catalyzed C-N couplings of hydrazine-derived nucleophiles provide a powerful alternative to Pd-catalyzed methods. This continuous-flow photochemical protocol, optimized using design of experiments, achieves these couplings in short residence times, with high selectivity. A range of (hetero)aryl bromides and chlorides are compatible and understanding of process stability/reactor fouling has been discerned. This journal is

INDAZOLONE ANALOGS AS GLYCOGEN SYNTHASE ACTIVATORS

-

Page/Page column 10, (2011/05/16)

Provided herein are compounds of the formula (I): as well as pharmaceutically acceptable salts thereof, wherein the substituents are as those disclosed in the specification. These compounds, and the pharmaceutical compositions containing them, are useful

CuI/4-hydro-L-proline as a more effective catalytic system for coupling of aryl bromides with N-boc hydrazine and aqueous ammonia

Jiang, Liqin,Lu, Xu,Zhang, Hui,Jiang, Yongwen,Ma, Dawei

experimental part, p. 4542 - 4546 (2009/09/25)

(Chemical Equation Presented) CuI/4-hydroxy-L-proline-catalyzed coupling of aryl bromides and N-Boc hydrazine takes place in DMSO at 80°C to give N-aryl hydrazides. When aryl iodides are employed, this reaction completes at 50°C and no ligand is required. Under the catalysis of CuI/4-hydroxy-L- proline, the coupling reaction of aqueous ammonia with aryl bromides proceeds smoothly at 50°C to afford primary arylamines. In this case K 2CO3 is found as a better base than Cs2CO 3. These processes allow assembly of N-aryl hydrazides and primary arylamines that bear a wide range of functional groups including hydroxyl, amine, trifluoromethyl, ester, nitro, and ketone.

Copper(I)-picolinic acid catalyzed N-arylation of hydrazides

Lam, Miu Suen,Lee, Hang Wai,Chan, Albert S.C.,Kwong, Fuk Yee

supporting information; scheme or table, p. 6192 - 6194 (2009/04/05)

An efficient copper-catalyzed carbon-nitrogen bond formation is described. The copper(I) complex with commercially available 2-picolinic acid ligand was found to be effective in N-arylation of N-Boc-hydrazine. This methodology offers a regioselective N-ar

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