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1-BOC-4-(3-FLUORO-BENZYLAMINO)-PIPERIDINE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

856933-07-8

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856933-07-8 Usage

Chemical class

Belongs to the piperidine class of compounds.

Structure

Contains a BOC (tert-butyloxycarbonyl) protecting group and a 3-fluoro-benzylamino group.

Use

Commonly used as a building block in organic synthesis.

Industry application

Widely used in the pharmaceutical industry for the preparation of various compounds.

Intermediate

Serves as a valuable intermediate for the development of potential drug candidates.

Protection

The BOC protecting group shields the amine functionality, allowing for selective reactions at other sites on the molecule.

Precursor

Often employed as a precursor in the synthesis of biologically active molecules.

Tool

A valuable tool for medicinal chemists in the development of new pharmaceuticals.

Check Digit Verification of cas no

The CAS Registry Mumber 856933-07-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,6,9,3 and 3 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 856933-07:
(8*8)+(7*5)+(6*6)+(5*9)+(4*3)+(3*3)+(2*0)+(1*7)=208
208 % 10 = 8
So 856933-07-8 is a valid CAS Registry Number.

856933-07-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl 4-[(3-fluorophenyl)methylamino]piperidine-1-carboxylate

1.2 Other means of identification

Product number -
Other names -

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:856933-07-8 SDS

856933-07-8Downstream Products

856933-07-8Relevant academic research and scientific papers

Design and synthesis of selective, small molecule inhibitors of coactivator-associated arginine methyltransferase 1 (CARM1)

Kaniskan,Eram,Liu,Smil,Martini,Shen,Santhakumar,Brown,Arrowsmith,Vedadi,Jin

, p. 1793 - 1796 (2016/09/28)

Coactivator-associated arginine methyltransferase 1 (CARM1) is a type I protein arginine methyltransferase (PRMT) that catalyzes the conversion of arginine into monomethylarginine (MMA) and further into asymmetric dimethylarginine (ADMA). CARM1 methylates histone 3 arginines 17 and 26, as well as numerous non-histone proteins including CBP/p300, SRC-3, NCOA2, PABP1, and SAP49, while also functioning as a coactivator for various proteins that have been linked to cancer such as p53, NF-κβ, β-catenin, E2F1 and steroid hormone receptor ERα. As a result, CARM1 is involved in transcriptional activation, cellular differentiation, cell cycle progression, RNA splicing and DNA damage response. It has been associated with several human cancers including breast, colon, prostate and lung cancers and thus, is a potential oncological target. Herein, we present the design and synthesis of a series of CARM1 inhibitors. Based on a fragment hit, we discovered compound 9 as a potent inhibitor that displayed selectivity for CARM1 over other PRMTs.

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