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Benzene, 1-(bromomethyl)-5-methoxy-2-nitro-4-(phenylmethoxy)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

64154-65-0

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64154-65-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 64154-65-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,1,5 and 4 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 64154-65:
(7*6)+(6*4)+(5*1)+(4*5)+(3*4)+(2*6)+(1*5)=120
120 % 10 = 0
So 64154-65-0 is a valid CAS Registry Number.

64154-65-0Relevant academic research and scientific papers

Preparation method, raw material, product and application of photo-crosslinking hydrogel material

-

, (2019/06/07)

The invention provides a preparation method, a raw material, a product and an application of a photo-crosslinking hydrogel material. The preparation method comprises the steps of dissolving a component A, namely a photosensitive high polymer derivative, i

Rapid and reversible hydrazone bioconjugation in cells without the use of extraneous catalysts

Nisal, Rahul,Jose, Gregor,Shanbhag, Chitra,Kalia, Jeet

, p. 4304 - 4310 (2018/06/22)

The amenability of hydrazone linkages to disassemble via either hydrolysis in mildly acidic aqueous solutions or transimination upon treatment with amine nucleophiles renders them extremely attractive for applications in chemical biology, drug delivery and materials science. Unfortunately, however, the use of hydrazones is hampered by the extremely slow intrinsic rates of their formation from their hydrazine and carbonyl precursors. Consequently, hydrazone formation is typically performed in the presence of a large excess of cytotoxic aniline-based nucleophilic catalysts, rendering hydrazones unsuitable for biological applications that entail their formation in cells. Herein, we report a hydrazine scaffold - o-amino benzyl hydrazine - that rapidly forms hydrazones via intramolecular nucleophilic catalysis, thereby obviating the use of extraneous catalysts. We demonstrate the use of this scaffold for rapid and reversible peptide and protein hydrazone bioconjugation and also for reversible fluorescent labeling of sialylated glycoproteins and choline lipids in mammalian cells.

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