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1379649-73-6

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1379649-73-6 Usage

Description

Thiol-PEG2-acid is a PEG linker containing a thiol group and a terminal carboxylic acid. The hydrophilic PEG spacer increases solubility in aqueous media. The thiol group reacts with maleimide, OPSS, vinylsulfone and transition metal surfaces including gold, silver, etc. The terminal carboxylic acid can react with primary amine groups in the presence of activators (e.g. EDC, or HATU) to form a stable amide bond.

Check Digit Verification of cas no

The CAS Registry Mumber 1379649-73-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,9,6,4 and 9 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1379649-73:
(9*1)+(8*3)+(7*7)+(6*9)+(5*6)+(4*4)+(3*9)+(2*7)+(1*3)=226
226 % 10 = 6
So 1379649-73-6 is a valid CAS Registry Number.

1379649-73-6Downstream Products

1379649-73-6Relevant articles and documents

Rapid preparation of multifunctional surfaces for orthogonal ligation by microcontact chemistry

Wendeln, Christian,Rinnen, Stefan,Schulz, Christian,Kaufmann, Tobias,Arlinghaus, Heinrich F.,Ravoo, Bart Jan

, p. 5880 - 5888 (2012/07/01)

Microcontact chemistry has been applied to patterned glass and silicon substrates by successive reaction of unprotected and monoprotected heterobifunctional linkers with alkene-terminated self-assembled monolayers (SAMs) to produce bi-, tri-, and tetrafunctional surfaces. Photochemical microcontact printing of an azide thiol linker followed by immobilization of an acid thiol linker on an undecenyl-terminated SAM results in a well-defined, micropatterned surface with terminal azide, acid, and alkene groups. Biologically relevant molecules (biotin, carbohydrates) have been selectively attached to the surface by means of orthogonal ligation chemistry, and the resulting microarrays display selective binding to fluorescently labeled proteins. An orthogonally addressable, tetrafunctional surface (azide, acid, alkene, and amine) can be prepared by an additional printing step of a tert-butyloxycarbonyl (Boc)-protected alkyne amine linker on the azide structures by using the copper(I)-catalyzed azide-alkyne Huisgen cycloaddition and subsequent removal of the protective group. Copyright

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