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2-Piperidinemethanol, 6-dodecyl-3-(phenylmethoxy)-, (2S,3R,6R)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

849428-89-3

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849428-89-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 849428-89-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,9,4,2 and 8 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 849428-89:
(8*8)+(7*4)+(6*9)+(5*4)+(4*2)+(3*8)+(2*8)+(1*9)=223
223 % 10 = 3
So 849428-89-3 is a valid CAS Registry Number.

849428-89-3SDS

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 [(2S,3R,6R)-6-dodecyl-3-phenylmethoxypiperidin-2-yl]methanol

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:849428-89-3 SDS

849428-89-3Downstream Products

849428-89-3Relevant academic research and scientific papers

A short synthesis of (-)-deoxoprosophylline

Jourdant, Angelique,Zhu, Jieping

, p. 249 - 259 (2007/10/03)

Syntheses of (-)-deoxoprosophylline from chiral L-N,N-dibenzylserine (TBDMS) aldehyde is reported. A highly diastereoselective nucleophilic addition of Buechi's Grignard reagent to chiral serinal followed by an intramolecular reductive amination of ω-oxo

Asymmetric total synthesis of (-)-deoxoprosophylline

Jourdant, Angélique,Zhu, Jieping

, p. 3431 - 3434 (2007/10/03)

Asymmetric syntheses of (-)-deoxoprosophylline from chiral L-N,N-dibenzyl serine (TBDMS) aldehyde is reported. A highly diastereoselective intramolecular reductive amination of ω-oxo amino diol is a key step of the present synthesis.

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