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(S)-N-BOC-LEUCINE-NITRILE is a chemical compound that belongs to the class of nitriles, characterized by the presence of a cyano group (-C≡N). It is a derivative of leucine, an essential amino acid crucial for protein synthesis and maintaining overall human health. The BOC (tert-butyloxycarbonyl) group in its structure serves as a protecting group in organic synthesis, temporarily masking reactive functional groups such as amines to prevent unwanted reactions. (S)-N-BOC-LEUCINE-NITRILE holds potential in medicinal chemistry and drug development, acting as a building block for synthesizing a variety of pharmaceutical compounds, and its nitrile functionality makes it a valuable intermediate for preparing other nitrogen-containing organic molecules.

115654-61-0

115654-61-0 Suppliers

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115654-61-0 Usage

Uses

Used in Medicinal Chemistry:
(S)-N-BOC-LEUCINE-NITRILE is used as a building block for the synthesis of pharmaceutical compounds, contributing to the development of new drugs with potential therapeutic applications.
Used in Drug Development:
In the pharmaceutical industry, (S)-N-BOC-LEUCINE-NITRILE is utilized as a key intermediate in the preparation of nitrogen-containing organic molecules, which are essential components in the creation of various medicinal agents.
Used in Organic Synthesis:
(S)-N-BOC-LEUCINE-NITRILE is employed as a protecting group in organic synthesis to temporarily mask reactive functional groups, facilitating controlled reactions and enhancing the yield of desired products.

Check Digit Verification of cas no

The CAS Registry Mumber 115654-61-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,6,5 and 4 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 115654-61:
(8*1)+(7*1)+(6*5)+(5*6)+(4*5)+(3*4)+(2*6)+(1*1)=120
120 % 10 = 0
So 115654-61-0 is a valid CAS Registry Number.

115654-61-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name (S)-N-BOC-LEUCINE-NITRILE

1.2 Other means of identification

Product number -
Other names Boc-Ile-Nitrile

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:115654-61-0 SDS

115654-61-0Downstream Products

115654-61-0Relevant academic research and scientific papers

Photoinduced direct cyanation of C(sp3)-H bonds

Hoshikawa, Tamaki,Yoshioka, Shun,Kamijo, Shin,Inoue, Masayuki

, p. 874 - 887 (2013/05/09)

A general and practical synthetic protocol for the direct transformation of unreactive C(sp3)-H bonds to C(sp3)-CN bonds has been developed. The homolytic cleavage of the C-H bond is initiated by photo-excited benzophenone, and the resulting carbon radical subsequently reacts with tosyl cyanide to afford the corresponding nitrile in a highly efficient manner. The present methodology is widely applicable to various starting materials including ethers, alcohols, amine derivatives, alkanes, and alkylbenzenes. This newly developed C-H cyanation protocol provides a powerful tool for selective one-carbon elongation for the construction of architecturally complex molecules. Georg Thieme Verlag Stuttgart - New York.