95388-79-7

Usage

Uses

Used in Pharmaceutical Industry:
Tert-Butyl 4-chlorobutylcarbamate is used as a protecting group for amine functional groups during chemical synthesis, ensuring that these groups remain intact and unreacted until the protective group is intentionally removed. This selective protection is crucial for the successful synthesis of complex pharmaceutical compounds.
Used in Peptide Synthesis:
In the field of peptide synthesis, tert-Butyl 4-chlorobutylcarbamate is employed as a protecting agent for amine groups. Its easy removal under mild conditions allows for the controlled deprotection of amine groups at specific stages of the synthesis process, facilitating the stepwise assembly of peptide chains.
Used in Specialty Chemicals Production:
Tert-Butyl 4-chlorobutylcarbamate is utilized in the production of specialty chemicals, where its protective properties are harnessed to control the reactivity of amine groups during the synthesis of various chemical products.
Used in Agrochemicals Production:
Similarly, in the agrochemicals industry, tert-Butyl 4-chlorobutylcarbamate is used to protect amine groups during the synthesis of active ingredients for pesticides and other agricultural chemicals, ensuring the successful creation of desired products with specific biological activities.

InChI:InChI=1/C9H18ClNO2/c1-9(2,3)13-8(12)11-7-5-4-6-10/h4-7H2,1-3H3,(H,11,12)

Upstream product

• 58885-58-8 N-tert-butoxycarbonyl-3-aminopropanol 
• 75178-87-9 (4-hydroxybutyl)carbamic acid tert-butyl ester 
• 75178-90-4 N-(tert-butyloxycarbonyl)-5-aminopentanol 
• 174626-25-6 methanesulfonic acid 4-tert-butoxycarbonylaminobutyl ester 
• 75844-69-8 t-butyl piperidinecarboxylate 
• 24424-99-5 di-tert-butyl dicarbonate 

Relevant academic research and scientific papers

DECONSTRUCTIVE FUNCTIONALIZATION METHODS AND COMPOUNDS

Disclosed herein, inter alia, are deconstructive functionalization methods and compounds made using the same.

Rapid Assembly of Saturated Nitrogen Heterocycles in One-Pot: Diazo-Heterocycle “Stitching” by N–H Insertion and Cyclization

Methods that provide rapid access to new heterocyclic structures in biologically relevant chemical space provide important opportunities in drug discovery. Here, a strategy is described for the preparation of 2,2-disubstituted azetidines, pyrrolidines, pi

ORGANIC COMPOUNDS

A compound of formula (I) or tautomers, or stereoisomers, or solvates, or pharmaceutically acceptable salts thereof, wherein M1, M1, L1, L2, W1, W2, X1, X2, Y1, Y2, A, R5 and R5a are as defined herein for the for treatment of conditions mediated by the blockade of an epithelial sodium channel, particularly an inflammatory or allergic condition.

CHEMICAL COMPOUNDS

The present invention provides novel compounds that demonstrate protective effects on target cells from HIV infection in a manner as to bind specifically to the chemokine receptor, and which affect the binding of the natural ligand or chemokine to a receptor such as CXCR4 and/or CCR5 of a target cell.

Malonic acid derivatives and methods for their synthesis

The present invention refers to a new class of malonic acid derivatives of general formula I STR1 wherein R1 and R2, each independently, represent hydrogen or a carboxyl protecting group, and the residue R corresponds to the side-cha