Welcome to LookChem.com Sign In|Join Free
  • or
TERT-BUTYL 4-(BENZYLOXYMETHYL)-4-CYANOPIPERIDINE-1-CARBOXYLATE is a chemical compound with the molecular formula C21H29N3O3. It is a tertiary butyl ester derivative of piperidine carboxylic acid, featuring a benzyloxymethyl group and a cyano group. TERT-BUTYL 4-(BENZYLOXYMETHYL)-4-CYANOPIPERIDINE-1-CARBOXYLATE is primarily utilized as a building block in organic synthesis, especially in the pharmaceutical industry for the development of various drugs. Its potential applications in the synthesis of therapeutically relevant molecules highlight its importance in medicinal chemistry, although the specific uses may differ based on the context. Due to its chemical nature, it is crucial for researchers and chemists to handle TERT-BUTYL 4-(BENZYLOXYMETHYL)-4-CYANOPIPERIDINE-1-CARBOXYLATE with appropriate safety measures to mitigate any potential hazards.

919284-64-3

Post Buying Request

919284-64-3 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

919284-64-3 Usage

Uses

Used in Pharmaceutical Industry:
TERT-BUTYL 4-(BENZYLOXYMETHYL)-4-CYANOPIPERIDINE-1-CARBOXYLATE is used as a building block in organic synthesis for the production of various drugs. It serves as a key intermediate in the development of molecules with potential therapeutic properties, contributing to the advancement of new pharmaceutical agents.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, TERT-BUTYL 4-(BENZYLOXYMETHYL)-4-CYANOPIPERIDINE-1-CARBOXYLATE is employed as a valuable component in the synthesis of bioactive compounds. Its structural features allow for the creation of diverse chemical entities that can be further optimized for improved pharmacological activity and selectivity.
Used in Drug Discovery and Development:
TERT-BUTYL 4-(BENZYLOXYMETHYL)-4-CYANOPIPERIDINE-1-CARBOXYLATE is utilized in drug discovery and development processes to create novel chemical entities with potential therapeutic applications. Its unique structural elements can be leveraged to design and synthesize new drug candidates that address unmet medical needs.

Check Digit Verification of cas no

The CAS Registry Mumber 919284-64-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,9,2,8 and 4 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 919284-64:
(8*9)+(7*1)+(6*9)+(5*2)+(4*8)+(3*4)+(2*6)+(1*4)=203
203 % 10 = 3
So 919284-64-3 is a valid CAS Registry Number.

919284-64-3SDS

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-cyano-4-(phenylmethoxymethyl)piperidine-1-carboxylate

1.2 Other means of identification

Product number -
Other names 1-Piperidinecarboxylic acid,4-cyano-4-[(phenylmethoxy)methyl]-,1,1-dimethylethyl ester

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:919284-64-3 SDS

919284-64-3Relevant academic research and scientific papers

HETEROCYCLIC COMPOUNDS CONTAINING AN INDOLE CORE

-

Page/Page column 86, (2011/06/26)

Disclosed are novel compounds which inhibit RSK, methods of making such compounds and pharmaceutical compositions comprising such compounds. Also disclosed are methods of treating RSK2 regulated disorders using compounds of the invention.

Synthesis and SAR of GlyT1 inhibitors derived from a series of N-((4-(morpholine-4-carbonyl)-1-(propylsulfonyl)piperidin-4-yl)methyl)benzamides

Zhao, Zhijian,O'Brien, Julie A.,Lemaire, Wei,Williams Jr., David L.,Jacobson, Marlene A.,Sur, Cyrille,Pettibone, Doug J.,Tiller, Philip R.,Smith, Sheri,Hartman, George D.,Wolkenberg, Scott E.,Lindsley, Craig W.

, p. 5968 - 5972 (2007/10/03)

This Letter describes the synthesis and SAR, developed through an iterative analog library approach, of potent and selective non-sarcosine-derived GlyT1 inhibitors.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 919284-64-3