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170491-61-9

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170491-61-9 Usage

Description

1-Boc-2-(2-Oxoethyl)Piperidine is a chemical compound with the molecular formula C13H24N2O3. It is a derivative of piperidine and is commonly used in organic synthesis as a protecting group for amines. 1-Boc-2-(2-Oxoethyl)Piperidine features a Boc (tert-butoxycarbonyl) group at the nitrogen atom and a 2-oxoethyl group at the piperidine ring, which makes it a valuable building block for the synthesis of various pharmaceuticals and organic compounds. 1-Boc-2-(2-Oxoethyl)Piperidine is stable under standard lab conditions and can be stored without decomposition for extended periods. It is a versatile compound that has numerous applications in the field of medicinal chemistry and drug discovery.

Uses

Used in Pharmaceutical Industry:
1-Boc-2-(2-Oxoethyl)Piperidine is used as a building block for the synthesis of various pharmaceuticals and organic compounds. Its unique structure allows for the creation of a wide range of molecules with potential therapeutic applications.
Used in Medicinal Chemistry:
1-Boc-2-(2-Oxoethyl)Piperidine is used as a protecting group for amines in organic synthesis, which is crucial for the development of new drugs and the modification of existing ones. Its ability to protect amines during chemical reactions ensures that the desired products are formed without unwanted side reactions.
Used in Drug Discovery:
1-Boc-2-(2-Oxoethyl)Piperidine is used in the field of drug discovery to facilitate the synthesis of new compounds with potential therapeutic properties. Its versatility and stability make it an ideal candidate for use in the development of novel drugs and drug candidates.

Check Digit Verification of cas no

The CAS Registry Mumber 170491-61-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,0,4,9 and 1 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 170491-61:
(8*1)+(7*7)+(6*0)+(5*4)+(4*9)+(3*1)+(2*6)+(1*1)=129
129 % 10 = 9
So 170491-61-9 is a valid CAS Registry Number.

170491-61-9SDS

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 2-(2-oxoethyl)piperidine-1-carboxylate

1.2 Other means of identification

Product number -
Other names QC-7303

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:170491-61-9 SDS

170491-61-9Relevant articles and documents

Synthesis of Azocanes from Piperidines via an Azetidinium Intermediate

Leverenz, Malte,Masson, Guillaume,Pardo, Domingo Gomez,Cossy, Janine

, p. 16325 - 16328 (2021/10/25)

α-Trifluoromethyl azocanes are accessible from 2-(trifluoropropan-2-ol) piperidines by metal-free ring-expansion involving a bicyclic azetidinium intermediate. The opening of the azetidinium intermediate was achieved by various nucleophiles (amines, alcoholates, carboxylates, phosphonates, halides and pseudo-halides) with an excellent regio- diastereo- and enantioselectivity and in good yields. The relative configuration of the piperidines and azocanes were assigned and the deprotected azocanes offer opportunities for further derivatization.

USE OF AMINOINDANE COMPOUNDS IN TREATING OVERACTIVE BLADDER AND INTERSTITIAL CYSTITIS

-

, (2014/03/22)

The present application provides methods of using the aminoindane compounds of formula (I) or (II) in treating an overactive bladder or interstitial cystitis by administering one or more of the compounds to a patient.

Substituted Spiroamine Compounds

-

, (2010/05/13)

Substituted spiroamine compounds corresponding to the formula (I) In which m, n, o, p, Q, r, s, t, R1, R2, R3, R4a, R4b, R5a, R5b, R6a, R6b, R7, R8, R9, R10 and R11 have defined meanings; a process for the preparation of such compounds, pharmaceutical compositions containing such compounds and the use of substituted spiroamines for the treatment or inhibition of pain and/or other conditions mediated by the bradykinin 1 receptor.

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