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1H-Imidazole, 1-(2-iodobenzoyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

481075-70-1

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481075-70-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 481075-70-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,8,1,0,7 and 5 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 481075-70:
(8*4)+(7*8)+(6*1)+(5*0)+(4*7)+(3*5)+(2*7)+(1*0)=151
151 % 10 = 1
So 481075-70-1 is a valid CAS Registry Number.

481075-70-1Relevant academic research and scientific papers

Dearomatization through Photoredox Hydroarylation: Discovery of a Radical-Polar Crossover Strategy

Jui, Nathan T.,McDaniel, Kelly A.

supporting information, p. 5576 - 5580 (2021/07/31)

Indole dearomatization has been achieved via radical hydroarylation. Under mild photoredox conditions, a range of indole derivatives undergo hydroarylation to form 2-arylindoline products. Mechanistically, radical termination occurs primarily via stepwise

Indium-mediated one-pot synthesis of benzoxazoles or oxazoles from 2-nitrophenols or 1-aryl-2-nitroethanones

Lee, Jung June,Kim, Jihye,Jun, Young Moo,Lee, Byung Min,Kim, Byeong Hyo

experimental part, p. 8821 - 8831 (2009/12/26)

One-pot reduction-triggered heterocyclizations from 2-nitrophenols to benzoxazoles and from 1-aryl-2-nitroethanones to oxazoles were investigated. In the presence of indium/AcOH in benzene at reflux, 2-nitrophenols and R-C(OMe)3 (R=H, Me, Ph) produced excellent yields of corresponding benzoxazoles within an hour. Similarly, 1-aryl-2-nitroethanones and Ph-C(OMe)3 in the presence of indium/AcOH in acetonitrile transformed into the corresponding oxazoles with good yields.

Stability studies of N-acylimidazoles

Zaramella, Simone,Stroemberg, Roger,Yeheskiely, Esther

, p. 2633 - 2639 (2007/10/03)

Studies of the stabilities of a series of N-acylimidazoles towards acidic and basic conditions of potential usefulness for the removal of common temporary protection in peptide and oligonucleotide synthesis are presented. N-Acylimidazoles with a variety of substituents in the acyl component were prepared and treated with 3% trifluoroacetic acid (TFA) in chloroform and with 2% 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) in N,N-dimethylformamide (DMF), the extent of their degradation being determined by proton NMR. N-(2,4,6-Trimethylbenzoyl)imidazole (1) and N-(2,6-dimethoxybenzoyl)-imidazole (2) remained unaffected under the above acidic and basic conditions after 4 d and 2 d, respectively. In addition, 1 and 2 were resistant to treatment with a solution of 2% piperidine/2% DBU in DMF for 24 h. Under ammonolytic conditions, 2 was rapidly cleaved (less than 1 h), whereas 1 was 64% degraded after 48 h, as ascertained by reversed-phase HPLC. Wiley-VCH Verlag GmbH, 69451 Weinheim, Germany, 2002.

Potential organ- or tumor-imaging agents. XXII Acyl-labeled cholesterol esters

Seevers,Schwendner,Swayze,Counsell

, p. 618 - 621 (2007/10/02)

A series of cholesteryl phenylalkanoic esters was synthesized in which the acyl moiety served as the carrier for radioiodine. Tissue distribution studies in rats revealed that several of these radioiodinated esters selectively accumulated in steroid-secre

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