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(S)-4-(4-bromophenyl)-5-((tert-butoxycarbonyl)amino)pentyl methanesulfonate is a chemical compound that belongs to the class of methanesulfonates. It is characterized by a long alkyl chain with a terminal bromophenyl group and a t-butylcarbonyl-protected amine group. (S)-4-(4-bromophenyl)-5-((tert-butoxycarbonyl)amino)pentyl methanesulfonate is known for its utility in organic synthesis and its potential applications in the pharmaceutical industry.

1476776-66-5

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1476776-66-5 Usage

Uses

Used in Pharmaceutical Synthesis:
(S)-4-(4-bromophenyl)-5-((tert-butoxycarbonyl)amino)pentyl methanesulfonate is used as a reagent for the preparation of various pharmaceuticals and bioactive molecules. Its unique structure allows for the creation of complex organic molecules that can be utilized in the development of new drugs.
Used in Organic Synthesis:
In the field of organic synthesis, (S)-4-(4-bromophenyl)-5-((tert-butoxycarbonyl)amino)pentyl methanesulfonate is used as a building block for the construction of complex organic molecules. The t-butylcarbonyl-protected amine group can be deprotected to reveal the free amine, which is crucial in the synthesis of peptide and protein structures.
Used in Peptide and Protein Synthesis:
(S)-4-(4-bromophenyl)-5-((tert-butoxycarbonyl)amino)pentyl methanesulfonate is used as a key component in the synthesis of peptides and proteins. The deprotection of the t-butylcarbonyl group allows for the formation of amide bonds, which are essential for the structure and function of these biologically significant molecules.
Used in Bioactive Molecule Production:
(S)-4-(4-bromophenyl)-5-((tert-butoxycarbonyl)amino)pentyl methanesulfonate is also used in the production of bioactive molecules, which have the potential to interact with biological systems and exhibit pharmacological or biological effects. The methanesulfonate group serves as a good leaving group in synthetic reactions, making (S)-4-(4-bromophenyl)-5-((tert-butoxycarbonyl)amino)pentyl methanesulfonate a valuable asset in the development of such molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 1476776-66-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,7,6,7,7 and 6 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1476776-66:
(9*1)+(8*4)+(7*7)+(6*6)+(5*7)+(4*7)+(3*6)+(2*6)+(1*6)=225
225 % 10 = 5
So 1476776-66-5 is a valid CAS Registry Number.

1476776-66-5Upstream product

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