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1158758-98-5

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1158758-98-5 Usage

General Description

Tert-butyl 4-(aminomethyl)-4-ethylpiperidine-1-carboxylate is a chemical compound with the molecular formula C15H28N2O2. It is a piperidine derivative that is commonly used in the synthesis of pharmaceuticals and organic compounds. tert-butyl 4-(aMinoMethyl)-4-ethylpiperidine-1-carboxylate has a tertiary butyl functional group, an aminomethyl group, and an ethyl group attached to the piperidine ring, as well as a carboxylate group. It is used as a building block in organic chemistry and can be utilized in the development of new drugs and research compounds. Its unique structure and properties make it an important intermediate in the field of medicinal chemistry and drug discovery.

Check Digit Verification of cas no

The CAS Registry Mumber 1158758-98-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,5,8,7,5 and 8 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1158758-98:
(9*1)+(8*1)+(7*5)+(6*8)+(5*7)+(4*5)+(3*8)+(2*9)+(1*8)=205
205 % 10 = 5
So 1158758-98-5 is a valid CAS Registry Number.

1158758-98-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl 4-(aminomethyl)-4-ethylpiperidine-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:1158758-98-5 SDS

1158758-98-5Downstream Products

1158758-98-5Relevant articles and documents

Non-aromatic A-ring replacement in the triaryl bis-sulfone CB2 receptor inhibitors

Gilbert, Eric J.,Zhou, Guowei,Wong, Michael K.C.,Tong, Ling,Shankar, Bandarpalle B.,Huang, Chunli,Kelly, Joseph,Lavey, Brian J.,McCombie, Stuart W.,Chen, Lei,Rizvi, Razia,Dong, Youhao,Shu, Youheng,Kozlowski, Joseph A.,Shih, Neng-Yang,Hipkin, R. William,Gonsiorek, Waldemar,Malikzay, Asra,Lunn, Charles A.,Favreau, Len,Lundell, Daniel J.

scheme or table, p. 608 - 611 (2010/05/02)

The triaryl bis-sulfone 1 was modified by converting the aryl A-ring to a piperidine ring. The piperidine ring was further elaborated to a spirocyclopropyl piperidine moiety. The effect on CB2 binding potency, rat calcium channel affinity, and CYP 2C9 inh

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