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14058-38-9

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14058-38-9 Usage

Description

Closely allied to the two preceding alkaloids, this base is also obtained from the leaves of Prosopis africana Taub. It furnishes colourless crystals from Me2CO and has [el:]D + 25° (CHC13). The structure is 3-hydroxy-6-(11-hydroxydedecyl)-2- hydroxymethylpiperidine.

References

Khuong-Huu et ai., Bull. Soc. Chim. Belg., 81,425 (972)

Check Digit Verification of cas no

The CAS Registry Mumber 14058-38-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,0,5 and 8 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 14058-38:
(7*1)+(6*4)+(5*0)+(4*5)+(3*8)+(2*3)+(1*8)=89
89 % 10 = 9
So 14058-38-9 is a valid CAS Registry Number.
InChI:InChI=1/C18H37NO3/c1-15(21)10-8-6-4-2-3-5-7-9-11-16-12-13-18(22)17(14-20)19-16/h15-22H,2-14H2,1H3

14058-38-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-(11-hydroxydodecyl)-2-(hydroxymethyl)piperidin-3-ol

1.2 Other means of identification

Product number -
Other names Prosopin

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:14058-38-9 SDS

14058-38-9Downstream Products

14058-38-9Relevant articles and documents

A configurational switch based on iridium-catalyzed allylic cyclization: Application in asymmetric total syntheses of prosopis, dendrobate, and spruce alkaloids

Gnamm, Christian,Broedner, Kerstin,Krauter, Caroline M.,Helmchen, Guenter

experimental part, p. 10514 - 10532 (2010/04/29)

A method for the stereoselective synthesis of 2,6-disubstituted piperidines has been developed that is based on the use of an intramolecular iridium-catalyzed allylic substitution as a configurational switch. The procedure allows the preparation of 2-viny

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