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(E)-4-((4-chloro-6-((4-(2-cyanovinyl)-2,6-dimethylphenyl)amino)-1,3,5-triazin-2-yl)amino)benzonitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1458666-40-4

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1458666-40-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1458666-40-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,5,8,6,6 and 6 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1458666-40:
(9*1)+(8*4)+(7*5)+(6*8)+(5*6)+(4*6)+(3*6)+(2*4)+(1*0)=204
204 % 10 = 4
So 1458666-40-4 is a valid CAS Registry Number.

1458666-40-4Relevant academic research and scientific papers

Triazines With Suitable Spacers for Treatment And/Or Prevention of HIV Infections

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Paragraph 0240; 0242, (2015/05/13)

The present invention relates to the field of HIV-1 infections, and in particular provides novel compounds containing triazine rings and suitable spacers. The compounds according to this invention are very suitable for the prevention and/or treatment of H

TRIAZINES WITH SUITABLE SPACERS FOR TREATMENT AND/OR PREVENTION OF HIV INFECTIONS

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Page/Page column 27, (2013/10/08)

The present invention relates to the field of HIV-1 infections, and in particular provides novel compounds containing triazine rings and suitable spacers. The compounds according to this invention are very suitable for the prevention and/or treatment of H

Optimization of diarylazines as anti-HIV agents with dramatically enhanced solubility

Bollini, Mariela,Cisneros, José A.,Spasov, Krasimir A.,Anderson, Karen S.,Jorgensen, William L.

, p. 5213 - 5216 (2013/09/12)

Non-nucleoside inhibitors of HIV-1 reverse transcriptase are reported that have ca. 100-fold greater solubility than the structurally related drugs etravirine and rilpivirine, while retaining high anti-viral activity. The solubility enhancements come from strategic placement of a morpholinylalkoxy substituent in the entrance channel of the NNRTI binding site. Compound 4d shows low-nanomolar activity similar to etravirine towards wild-type HIV-1 and key viral variants.

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