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2-Chloro-3-(4-methylpiperazinonaphthoquinone) is a chemical compound with the molecular formula C17H16ClN3O2. It is a derivative of naphthoquinone, featuring a chloro group at the 2-position and a 4-methylpiperazine group at the 3-position. 2-CHLORO-3-(4-METHYLPIPERAZINO)NAPHTHOQUINONE is known for its potential applications in the synthesis of pharmaceuticals and other organic compounds. It is characterized by its yellowish color and is typically used as an intermediate in chemical reactions. Due to its specific functional groups, it can participate in various chemical transformations, making it a valuable component in the field of organic chemistry and drug development.

6312-48-7

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6312-48-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6312-48-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,1 and 2 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6312-48:
(6*6)+(5*3)+(4*1)+(3*2)+(2*4)+(1*8)=77
77 % 10 = 7
So 6312-48-7 is a valid CAS Registry Number.
InChI:InChI=1/C15H15ClN2O2/c1-17-6-8-18(9-7-17)13-12(16)14(19)10-4-2-3-5-11(10)15(13)20/h2-5H,6-9H2,1H3

6312-48-7Downstream Products

6312-48-7Relevant academic research and scientific papers

Reactions of quinones with some amino alcohols, thiols and a UV-Vis study

Ibis, Cemil,Sahinler Ayla, Sibel,Babayeva, Elvira

, p. 474 - 480 (2020)

In the present study, the reactions of 2,3-dichloro-1,4-naphthoquinone (DCNQ) with amino-1,2-propanediol and some thiols were investigated. Novel N-, N,S-, and S,O- substituted derivatives were obtained and the structures of all compounds were characteriz

An investigation of nucleophilic substitution reactions of 2,3-dichloro-1,4-naphthoquinone with various nucleophilic reagents

Ibis, Cemil,Shntaif, Ahmed Hassen,Bahar, Hakan,Sahinler Ayla, Sibel

, p. 731 - 738 (2015/08/24)

Novel N-, N,S- and N,O-substituted naphthoquinone compounds were prepared by the reactions of 2,3-dichloro-1,4-naphthoquinone (1) and the corresponding nucleophiles in the presence of chloroform and triethylamine or an ethanolic solution of Na2

NAPHTHAQUINONE METHYLTRANSFERASE INHIBITORS AND USES THEREOF

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Page/Page column 87; 88; 92, (2015/11/27)

Provided herein are compounds of (I), and pharmaceutically acceptable salts, solvates, hydrates, polymorphs, co-crystals, tautomers, stereoisomers, and prodrugs thereof. Also provided are pharmaceutical compositions and methods involving the inventive compounds for the treatment of proliferative diseases (e.g., cancer (e.g., leukemia, breast cancer, melanoma, metastatic cancer) and diseases associated with inappropriate SET8 activity. Also provided are methods for inhibiting SET8 and methods for labelling SET8.

Synthesis of photoactive 1-methyl-1-R-4-(1,4-dioxo-1,4-dihydronaphthalen-2- yl)piperazinium salts

Berezhnaya,Shelkovnikov,Korotaev

experimental part, p. 1823 - 1831 (2012/03/10)

Photoactive 4-(1,4-dioxo-1,4-dihydronaphthalen-2-yl)piperazinium salts were synthesized by alkylation of 3-chloro-2-(piperazin-1-yl)- and 2-arylamino-3-(4-methylpiperazin-1-yl)-1,4-naphthoquinones. Light sensitivities of materials obtained by adsorption o

'On water' assisted synthesis and biological evaluation of nitrogen and sulfur containing hetero-1,4-naphthoquinones as potent antifungal and antibacterial agents

Tandon, Vishnu K.,Maurya, Hardesh K.,Verma, Manoj K.,Kumar, Rohitashw,Shukla, Praveen K.

scheme or table, p. 2418 - 2426 (2010/07/05)

2-Chloro-3-(4-methylpiperazin-1-yl)naphthalene-1,4-dione (3a), 2-chloro-3-(pyrrolidin-1-yl)naphthalene-1,4-dione (3b), 2-chloro-3-(piperidin-1-yl)naphthalene-1,4-dione (3c), 2-chloro-3-morpholinonaphthalene-1,4-dione (3d), 2-chloro-3-(2-phenylhydrazinyl)n

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