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TERT-BUTYL 4-[(2Z)-2-AMINO-2-(HYDROXYIMINO)ETHYL]PIPERIDINE-1-CARBOXYLATE is a white solid chemical compound belonging to the piperidine family. It is derived from tert-butyl 4-oxopiperidine-1-carboxylate and has a molecular formula of C13H24N2O3 with a molecular weight of 256.34 g/mol. Its structural features and functional groups may contribute to its pharmacological properties, making it a promising candidate for applications in the pharmaceutical industry, organic synthesis, and medicinal chemistry. Further research and evaluation are required to fully understand its properties and potential applications.

713147-49-0

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713147-49-0 Usage

Uses

Used in Pharmaceutical Industry:
TERT-BUTYL 4-[(2Z)-2-AMINO-2-(HYDROXYIMINO)ETHYL]PIPERIDINE-1-CARBOXYLATE is used as a pharmaceutical compound for its potential pharmacological properties due to its structural features and functional groups.
Used in Organic Synthesis:
TERT-BUTYL 4-[(2Z)-2-AMINO-2-(HYDROXYIMINO)ETHYL]PIPERIDINE-1-CARBOXYLATE is used as a chemical intermediate in organic synthesis processes, contributing to the development of new compounds and materials.
Used in Medicinal Chemistry:
TERT-BUTYL 4-[(2Z)-2-AMINO-2-(HYDROXYIMINO)ETHYL]PIPERIDINE-1-CARBOXYLATE is used as a building block in medicinal chemistry for the design and synthesis of new drugs and therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 713147-49-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,1,3,1,4 and 7 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 713147-49:
(8*7)+(7*1)+(6*3)+(5*1)+(4*4)+(3*7)+(2*4)+(1*9)=140
140 % 10 = 0
So 713147-49-0 is a valid CAS Registry Number.

713147-49-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl 4-[(2Z)-2-amino-2-hydroxyiminoethyl]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:713147-49-0 SDS

713147-49-0Relevant academic research and scientific papers

5-HYDROXYPYRIMIDINE-4-CARBOXAMIDE DERIVATIVE

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, (2012/09/10)

The present invention provides a compound which enhances the production of erythropoietin. The present invention provides a compound represented by formula (1): [wherein, R1: formula (1A): [wherein, R4 and R5: H, halogen,

OXADIAZOLE COMPOUNDS, THEIR PREPARATION AND USE

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, (2011/09/30)

The present invention relates to oxadiazole compounds in all their stereoisomeric and tautomeric forms and mixtures thereof in all ratios; and their pharmaceutically acceptable salts, pharmaceutically acceptable solvates, pharmaceutically acceptable prodrugs and pharmaceutically acceptable polymorphs. The invention also relates to processes for the manufacture of the oxadiazole compounds and to pharmaceutical compositions containing them. The said compounds and their pharmaceutical compositions are useful in the treatment of cancer, particularly chronic myeloid leukemia (CML). The present invention further provides a method of treatment of cancer by administering a therapeutically effective amount of said compounds or their pharmaceutical compositions, to a mammal in need thereof.

5-HYDROXYPYRIMIDINE-4-CARBOXAMIDE COMPOUND

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, (2011/05/16)

The present invention provides compounds which promote erythropoietin production. Compounds represented by the following general formula (1) or pharmacologically acceptable salts thereof are provided: [wherein, R1 represents a group —X-Q1, X-Q1-Y-Q2 or X-Q1-Y-Q2-Z-Q3, X represents a single bond, —CH2— or the like, Q1 represents a monocyclic or bicyclic heterocyclic group which may have substituent(s), Y represents a single bond, —CH2—, or the like, Q2 represents a monocyclic or bicyclic hydrocarbon ring group which may have substituent(s) or a monocyclic or bicyclic heterocyclic group which may have substituent(s), Z represents a single bond, —CR11R12— or the like, R11 and R12 each independently represents a hydrogen atom, a halogen atom or the like, Q3 represents a phenyl group which may have substituent(s), a C3-C7 cycloalkyl group which may have substituent(s), a C3-C7 cycloalkenyl group which may have substituent(s) or a monocyclic or bicyclic heterocyclic group which may have substituent(s), R2 represents a C1-C3 alkyl group or the like, and R3 represents a hydrogen atom or a methyl group].

COMPOUNDS AND COMPOSITIONS AS MODULATORS OF GPR119 ACTIVITY

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Page/Page column 73, (2008/12/08)

The invention provides compounds, pharmaceutical compositions comprising such compounds and methods of using such compounds to treat or prevent diseases or disorders associated with the activity of GPR119.

Substituted homopiperidine, piperidine or pyrrolidine derivatives

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Page/Page column 26, (2010/02/11)

A novel class of substituted homopiperidine, piperidine and pyrrolidine derivatives, methods for their preparation, pharmaceutical compositions comprising them and use thereof in the treatment of disorders related to the histamine H3 receptor. More particularly, the compounds possess histamine H3 receptor antagonistic activity and are thus useful in the treatment of disorders in which a histamine H3 receptor blockade is beneficial.

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