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950482-79-8

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950482-79-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 950482-79-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,0,4,8 and 2 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 950482-79:
(8*9)+(7*5)+(6*0)+(5*4)+(4*8)+(3*2)+(2*7)+(1*9)=188
188 % 10 = 8
So 950482-79-8 is a valid CAS Registry Number.

950482-79-8Upstream product

950482-79-8Downstream Products

950482-79-8Relevant academic research and scientific papers

Piperidine compound and preparation method and medical application thereof

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Paragraph 0452-0457; 0458, (2021/04/07)

The invention discloses a piperidine compound shown as a formula (I) and a preparation method and medical application thereof, and particularly relates to a piperidine USP7 inhibitor compound or pharmaceutically acceptable salt or ester or solvate thereof and a preparation method and application of the piperidine USP7 inhibitor compound or pharmaceutically acceptable salt or ester or solvate thereof. The compound provided by the invention can inhibit the activity of USP7 enzyme, has very good selectivity and druggability, and can be used for preparing medicines for preventing or treating tumor diseases or virus infectious diseases.

Stereospecific 1,4-Metallate Shift Enables Stereoconvergent Synthesis of Ketoximes

Yang, Kai,Zhang, Feng,Fang, Tongchang,Zhang, Guan,Song, Qiuling

supporting information, p. 13421 - 13426 (2019/08/20)

Reported herein is a stereospecific 1,4-metallate rearrangement for single-geometry ketoxime synthesis from oxime chlorides and arylboronic acids. This strategy exhibits broad substrate scope with excellent stereoselectivity under mild reaction conditions. In comparison with the conventional approaches, each configuration of unsymmetric diaryl oximes, as well as the thermodynamically less stable Z isomer of aryl alkyl ketoximes can be selectively and exclusively obtained. The reactivities of unsymmetric diaryl oximes and the Z isomer of aryl alkyl oximes, a class of underexplored molecules, enables efficient access to the corresponding isoquinolines, isoquinoline N-oxides, and amides having a single configuration.

SUBSTITUTED ISOXAZOLINE COMPOUND AND PEST CONTROL AGENT

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Page/Page column 95, (2010/07/06)

There is provided a novel pest control agent, particularly an insecticide or miticide. A substituted isoxazoline compound of General Formula (1): where A1, A2 and A3 independently are CH or N, etc., X1, X2

SUBSTITUTED ISOXAZOLINE COMPOUND AND PEST CONTROL AGENT

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Page/Page column 206-207, (2009/01/20)

There is provided a novel pesticide, particularly an insecticide or an acaricide. A substituted isoxazoline compound of formula (1) or a salt thereof: wherein A1, A2and A3 independently of one another are carbon atom or nitrogen atom, G is benzene ring, etc., L is -CH2-, -C(CH3)-, -CH(CN)-, etc., X is halogen atom, C1-C6haloalkyl, etc., Y ia halogen atm, C1-C6alkyl, etc., R1 is -C(O)R1a, -C(O)OR1a, -C(O)NHR1a, etc., R2 is hydrogen atom, C1-C6haloalkyl, -C1-C4alkoxy C1-C4alkyl, cyano C1-C6alkyl, C3-C6alkenyl, C3-C6alkynyl, -C(O)R15, -C(O)OR15, etc., R3 is C1-C6haloalkyl, etc., m is an integer of 0 to 5, n is an integer of 0 to 4. The pesticide containing these compounds.

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