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methyl [2-(3-bromophenyl)-2-cyano]acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

895579-16-5

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895579-16-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 895579-16-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,5,5,7 and 9 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 895579-16:
(8*8)+(7*9)+(6*5)+(5*5)+(4*7)+(3*9)+(2*1)+(1*6)=245
245 % 10 = 5
So 895579-16-5 is a valid CAS Registry Number.

895579-16-5Downstream Products

895579-16-5Relevant academic research and scientific papers

ANTI-CD98 ANTIBODIES AND ANTIBODY DRUG CONJUGATES

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Page/Page column 381, (2018/01/15)

The invention relates to anti-CD98 antibodies and antibody drug conjugates (ADCs), including compositions and methods of using said antibodies and ADCs.

ANTI-EGFR ANTIBODY DRUG CONJUGATES

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Page/Page column 327, (2018/01/15)

The invention relates to anti-Epidermal Growth Factor Receptor (EGFR) antibody drug conjugates (ADCs) which inhibit Bcl-xL, including compositions and methods of using said ADCs.

BCL-XL Inhibitory Compounds and Antibody Drug Conjugates Including the Same

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Paragraph 0770, (2016/06/28)

Small molecule Bcl-xL inhibitors and Antibody Drug Conjugates (ADCs) comprising small molecule Bcl-xL inhibitors are disclosed herein. The Bcl-xL inhibitors and ADCs of the disclosure are useful for, among other things, inhibiting anti-apoptotic Bcl-xL proteins as a therapeutic approach towards the treatment of diseases that involve a dysregulated apoptosis pathway.

Acetone cyanohydrin as a source of HCN in the Cu-catalyzed hydrocyanation of α-aryl diazoacetates

Park, Eun Ju,Lee, Seungeon,Chang, Sukbok

supporting information; experimental part, p. 2760 - 2762 (2010/07/08)

A procedure for the Cu-catalyzed hydrocyanation of α-aryl diazoesters has been developed using acetone cyanohydrin as a source of hydrogen cyanide (HCN). It was found that the addition of trimethylsilyl cyanide (TMSCN) significantly accelerates the conversion presumably by delivering free cyanide ion in situ, thus producing various types of α-aryl cyanoacetates in high yields under mild conditions.

α,β-unsaturated β-silyl lmide substrates for catalytic, enantioselective conjugate additions: A total synthesis of (+)-lactacystin and the discovery of a new proteasome inhibitor

Balskus, Emily P.,Jacobsen, Eric N.

, p. 6810 - 6812 (2007/10/03)

Chiral (salen)Al μ-oxo dimer 1 catalyzes the highly enantioselective conjugate addition of carbon-centered nucleophiles to α,β-unsaturated silyl imides. Allyldimethylsilane-substituted imide 4 was identified as an optimal substrate, undergoing addition re

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