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5-bromo-1-phenyl-1H-indazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

861905-18-2

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861905-18-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 861905-18-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,1,9,0 and 5 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 861905-18:
(8*8)+(7*6)+(6*1)+(5*9)+(4*0)+(3*5)+(2*1)+(1*8)=182
182 % 10 = 2
So 861905-18-2 is a valid CAS Registry Number.

861905-18-2Relevant academic research and scientific papers

BTK INHIBITOR

-

, (2017/11/16)

Provided are a series of BTK inhibitors, and specifically disclosed are a compound, pharmaceutically acceptable salt thereof, tautomer thereof or prodrug thereof represented by formula (I), (II), (III) or (IV).

PLANT CIRCADIAN RHYTHM REGULATING AGENT

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Paragraph 0246-0248, (2016/10/08)

PROBLEM TO BE SOLVED: To provide a plant circadian rhythm regulating agent, and a more simple and convenient plant circadian rhythm regulating method. SOLUTION: A plant circadian rhythm regulating agent contains a heterocycle-containing compound represented by the general formula (1) or an agriculturally acceptable salt, hydrate or solvate thereof as an active ingredient. SELECTED DRAWING: None COPYRIGHT: (C)2016,JPOandINPIT

LIGHT-EMITTING MATERIAL FOR ORGANIC ELECTROLUMINESCENT DEVICE, ORGANIC ELECTROLUMINESCENT DEVICE USING SAME, AND MATERIAL FOR ORGANIC ELECTROLUMINESCENT DEVICE

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Paragraph 0350-0353, (2016/10/08)

Disclosed are a novel fused cyclic compound having excellent light emitting efficiency and thermal stability, a method for producing the same, and an organic electroluminescent device including the same compound. The fused cyclic compound is represented b

Pericyclic rearrangements of N-heterocyclic carbenes of indazole to substituted 9-aminoacridines

Guan, Zong,Wiechmann, Sascha,Drafz, Martin,Hübner, Eike,Schmidt, Andreas

, p. 3558 - 3567 (2013/06/05)

On deprotonation, 1-arylindazolium salts form 1-arylindazol-3-ylidenes which rearrange spontaneously via ring cleavage, ring closure and subsequent proton transfer to substituted 9-aminoacridines. By contrast, the N-heterocyclic carbene of 2-phenylindazol

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