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3-Piperidinecarboxylic acid, 1-(phenylsulfonyl)-, ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

349620-39-9

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349620-39-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 349620-39-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,9,6,2 and 0 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 349620-39:
(8*3)+(7*4)+(6*9)+(5*6)+(4*2)+(3*0)+(2*3)+(1*9)=159
159 % 10 = 9
So 349620-39-9 is a valid CAS Registry Number.

349620-39-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 1-(benzenesulfonyl)piperidine-3-carboxylate

1.2 Other means of identification

Product number -
Other names HMS1543E14

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:349620-39-9 SDS

349620-39-9Relevant academic research and scientific papers

Regioselective synthesis of 2-substituted 3-diarylmethylenylpiperidines

Chang, Meng-Yang,Lin, Chung-Han,Lee, Tein-Wei

, p. 627 - 631 (2012)

A simple three-step synthetic routes toward 2-substituted 3-diarylmethylenylpiperidines 7 (Y = CN) and 8 (Y = allyl) starting with 3-diarylmethylenylpiperidines 9 is described. The process was carried out by the bromomethoxylation of skeleton 9 with NBS i

N-substituted piperidines and their use as pharrmaceuticals

-

Page/Page column 41, (2010/02/15)

The present invention relates to inhibitors of 11-β hydroxyl steroid dehydrogenase type 1, antagonists of the mineralocorticoid receptor (MR), and pharmaceutical compositions thereof. The compounds of the invention can be useful in the treatment of various diseases associated with expression or activity of 11-β hydroxyl steroid dehydrogenase type 1 and/or diseases associated with aldosterone excess.

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