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162504-86-1

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162504-86-1 Usage

General Description

1-Boc-4-(2-ethoxycarbonylvinyl)piperidine is a chemical compound with the molecular formula C16H27NO3. It is a derivative of piperidine and contains a 1-boc protecting group as well as an ethoxycarbonylvinyl substituent. 1-Boc-4-(2-ethoxycarbonylvinyl)piperidine is commonly used in organic synthesis and medicinal chemistry as a building block for the synthesis of various compounds. It has been studied for its potential pharmacological properties, including its effects on the central nervous system and its potential as a therapeutic agent. Additionally, 1-Boc-4-(2-ethoxycarbonylvinyl)piperidine is known to have low toxicity and is considered to be a relatively safe chemical for handling and use in laboratory settings.

Check Digit Verification of cas no

The CAS Registry Mumber 162504-86-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,2,5,0 and 4 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 162504-86:
(8*1)+(7*6)+(6*2)+(5*5)+(4*0)+(3*4)+(2*8)+(1*6)=121
121 % 10 = 1
So 162504-86-1 is a valid CAS Registry Number.
InChI:InChI=1/C15H25NO4/c1-5-19-13(17)7-6-12-8-10-16(11-9-12)14(18)20-15(2,3)4/h6-7,12H,5,8-11H2,1-4H3/b7-6+

162504-86-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name t-butyl 4-(3-ethoxy-3-oxoprop-1-enyl)-tetrahydropyridine-1(2H)-carboxylate

1.2 Other means of identification

Product number -
Other names 40816 TERT-BUTYL 4-(3-ETHOXY-3-OXOPROP-1-ENYL)PIPERIDINE-1-CARBOXYLATE

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:162504-86-1 SDS

162504-86-1Relevant articles and documents

4 - piperidinyl - 1H - pyrrole - 3 - carboxamides hydrochloride synthetic method

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, (2017/08/25)

The invention discloses a synthesis method of 4-piperidyl-1H-pyrrole-3-formamide compound hydrochloride. The method comprises the following steps: reacting a compound I Boc-4-hydroxymethyl piperidine with oxalyl chloride to obtain a compound II, and reacting the compound II with triethyl phosphonoacetate to obtain a compound III; reacting the compound III with p-toluenesulfonylmethyl isocyanide to obtain a compound IV; reacting the compound IV with 2-(trimethylsilyl)-ethoxymethyl chloride to generate a compound V; hydrolyzing the compound V to obtain a compound VI, and reacting the compound VI with an amino compound to generate a compound VII; acting on the compound VII with tetrabutylammonium fluoride to generate a compound VIII; and acting on the compound VIII with HCI to generates a compound IX, namely 4-piperidyl-1H-pyrrole-3-formamide compound hydrochloride. According to the method, piperidyl and acylamino are introduced at the positions 3 and 4 on a pyrrole ring, the reaction route is simple and feasible, and the obtained compound has a plurality of reactive groups and good water solubility and has potentials for development of medical intermediates.

PIPERIDINYL COMPOUNDS THAT SELECTIVELY BIND INTEGRINS

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Page 83, (2010/11/30)

The invention is directed to piperidinyl compounds of formula (I) and (II) that selectively bind integrin receptors and methods for treating an integrin mediated disorder, wherein W, R2, Z and q are described in the application.

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