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5-(2-CHLOROBENZYL)-2-HYDROXYBENZALDEHYDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

328565-20-4

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328565-20-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 328565-20-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,8,5,6 and 5 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 328565-20:
(8*3)+(7*2)+(6*8)+(5*5)+(4*6)+(3*5)+(2*2)+(1*0)=154
154 % 10 = 4
So 328565-20-4 is a valid CAS Registry Number.

328565-20-4Relevant academic research and scientific papers

COMPOUNDS FOR USE IN THE TREATMENT OF ACUTE INTERMITTENT PORPHYRIA

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Page/Page column 38, (2021/05/29)

The invention provides compounds of formula (I), their pharmaceutically acceptable salts and prodrugs thereof for use in preventing, inhibiting or treating a disease caused by a mutation in the gene coding for hydroxymethylbilane synthase, in particular f

Structure-activity relationship study on col-003, a protein-protein interaction inhibitor between collagen and Hsp47

Yoshida, Masahito,Saito, Masazumi,Ito, Shinya,Ogawa, Koji,Goshima, Naoki,Nagata, Kazuhiro,Doi, Takayuki

, p. 220 - 226 (2020/11/26)

This study demonstrates the structure-activity relationship of Col-003, a potent collagen-heat-shock protein 47 (Hsp47) interaction inhibitor. Col-003 analogues were successfully synthesized by Pd(0)-catalyzed cross-coupling reactions of 5-bromosalicylald

Palladium- and nickel-catalyzed cross-couplings of unsaturated halides bearing relatively acidic protons with organozinc reagents

Manolikakes, Georg,Munoz Hernandez, Carmen,Schade, Matthias A.,Metzger, Albrecht,Knochel, Paul

supporting information; experimental part, p. 8422 - 8436 (2009/04/11)

(Chemical Equation Presented) A wide range of polyfunctional aryl, heteroaryl, alkyl, and benzylic zinc reagents were coupled with unsaturated aryl halides bearing an acidic NH or OH proton, using Pd(OAc)2 (1 mol %) and S-Phos (2 mol %) as catalyst without the need of protecting groups. A similar nickel-catalyzed reaction is described. The relative kinetic basicity of organozinc compounds as well as their stability toward acidic protons is also described.

Negishi cross-couplings of unsaturated halides bearing relatively acidic hydrogen atoms with organozinc reagents

Manolikakes, Georg,Schade, Matthias A.,Hernandez, Carmen Munoz,Mayr, Herbert,Knochel, Paul

supporting information; experimental part, p. 2765 - 2768 (2009/05/27)

(Chemical Equation Presented) A wide range of polyfunctional aryl, heteroaryl, alkyl, and benzylic zinc reagents were coupled with unsaturated halides bearing an acidic NH or OH function, using Pd(OAc)2 (1 mol %) and S-Phos (2 mol %) as catalyst without the need of protecting groups.

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