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182808-28-2

182808-28-2

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182808-28-2 Usage

Chemical Properties

Colourless Oil

Uses

Ethyl 4-Cyanopiperidine-1-carboxylate (cas# 182808-28-2) is a compound useful in organic synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 182808-28-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,2,8,0 and 8 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 182808-28:
(8*1)+(7*8)+(6*2)+(5*8)+(4*0)+(3*8)+(2*2)+(1*8)=152
152 % 10 = 2
So 182808-28-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H14N2O2/c1-2-13-9(12)11-5-3-8(7-10)4-6-11/h8H,2-6H2,1H3

182808-28-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name ETHYL 4-CYANOPIPERIDINE-1-CARBOXYLATE

1.2 Other means of identification

Product number -
Other names 4-Cyano-piperidine-1-carboxylic acid ethyl 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:182808-28-2 SDS

182808-28-2Downstream Products

182808-28-2Relevant articles and documents

Nickel-Catalyzed Cyanation of Unactivated Alkyl Sulfonates with Zn(CN)2

Xia, Aiyou,Lv, Peizhuo,Xie, Xin,Liu, Yuanhong

, p. 7842 - 7847 (2020/11/02)

Cyanation of unactivated primary and secondary alkyl mesylates with Zn(CN)2 catalyzed by nickel has been developed. The reaction provides an efficient route for the synthesis of alkyl nitriles with wide substrate scope, good functional group tolerance, and compatibility with heterocyclic compounds. Mechanistic studies indicate that alkyl iodide generated in situ serves as the reactive intermediate and the gradual release of alkyl iodide is crucial for the success of the reaction.

Preparation of spiro[cyclopent[b]indole-3,4'-piperidine] derivatives as acetylcholinesterase and monoamine oxidase inhibitors.

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, (2008/06/13)

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