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2-Cyanoethanesulfonyl chloride is a chemical compound characterized by the presence of a cyano group (-CN) and an ethanesulfonyl chloride group (-CH2-SO2-Cl). It is a versatile reagent in organic synthesis and has unique properties that make it suitable for various applications in different industries.

27869-05-2

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27869-05-2 Usage

Uses

Used in Pharmaceutical Industry:
2-Cyanoethanesulfonyl chloride is used as a protecting cap in oligonucleotide synthesis studies. It plays a crucial role in the synthesis of oligonucleotides, which are short DNA or RNA molecules with potential applications in gene therapy, diagnostics, and drug development. The protecting cap ensures the stability and integrity of the oligonucleotide during the synthesis process, preventing unwanted reactions and side products.
Used in Chemical Synthesis:
2-Cyanoethanesulfonyl chloride is also used as a reagent in various chemical synthesis processes. Its unique structure allows it to act as an electrophile, participating in reactions such as nucleophilic substitution and addition reactions. This makes it a valuable tool for the synthesis of complex organic molecules and pharmaceutical compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 27869-05-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,8,6 and 9 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 27869-05:
(7*2)+(6*7)+(5*8)+(4*6)+(3*9)+(2*0)+(1*5)=152
152 % 10 = 2
So 27869-05-2 is a valid CAS Registry Number.

27869-05-2Downstream Products

27869-05-2Relevant academic research and scientific papers

THE S- AND N-ADDITION OF THE COMPLEXES OF AMINES WITH SULFUR DIOXIDE TO ELECTROPHILIC ALKENES

Bodrikov, I. V.,Krasnov, V. L.,Samodurov, I. N.,Kazantsev, O. A.

, p. 923 - 928 (2007/10/02)

The addition of the complexes of amines with sulfur dioxide to acrylonitrile, methacrylonitrile, and crotononitrile was relized.The reactions of acrylonitrile with CH3NH2 -> SO2 and C2H5NH2 -> SO2 complexes take place with the formation of N-alkyl-2-cyanoethanesulfonamides (S-addition of the complexes at the double bond).The electrophilic alkenes react with (CH3)2NH -> SO2 and (C2H5)2NH -> SO2 to form complexes of the substituted β-aminonitriles with sulfur dioxide (N-addition of the complexes at the double bond).

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