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8α-hydroxy-13,14,15,16-tetranorlabdan-12-al is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

105014-29-7

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105014-29-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 105014-29-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,0,1 and 4 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 105014-29:
(8*1)+(7*0)+(6*5)+(5*0)+(4*1)+(3*4)+(2*2)+(1*9)=67
67 % 10 = 7
So 105014-29-7 is a valid CAS Registry Number.

105014-29-7SDS

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 [(1R,2R,4aS,8aS)-decahydro-2-hydroxy-2,5,5,8a-tetramethylnaphthalen-1-yl]ethanal

1.2 Other means of identification

Product number -
Other names 8α-hydroxy-13,14,15,16-tetranorlabdan-12-al

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:105014-29-7 SDS

105014-29-7Relevant academic research and scientific papers

Synthesis of pelorol and its analogs and their inhibitory effects on phosphatidylinositol 3-kinase

Luo, Yongjie,Chen, Huixuan,Weng, Jiang,Lu, Gui

, (2016/07/06)

There are numerous biologically active substances with novel structures and unique physiological functions in marine organisms. These substances are important sources of new lead compounds. Pelorol is a natural product isolated from marine organisms that possesses a novel structure with high bioactivity. In this paper, the synthesis of pelorol has been completed, and the synthesis of some intermediates has been optimized and scaled up. Five pelorol analogs have also been prepared. Preliminary biological activity testing demonstrated that compounds 5 and 6 might be potential lead compounds for cancer therapy.

PROCESS FOR THE CYCLODEHYDRATION OF DIOLS AND USE THEREOF FOR THE MANUFACTURING OF AMBRAFURAN AND OTHER CYCLOETHER DERIVATIVES

-

, (2013/03/26)

The present invention relates to a process for manufacturing tetrahydrofuran, tetrahydropyran and, more generally, cycloether derivatives through the cyclodehydration of 1,4- or 1,5- diols. More specifically, the process of the invention involves (i) the stereoselective cyclodehydration in water of 1,4- or 1,5- diols comprising at least one chiral tertiary alcohol functional group with retention of the initial chirality, and/or (ii) the cyclodehydration in water of 1,4- or 1,5- diols, said diols being non-miscible with and/or non-soluble in water, into corresponding cycloether derivatives, by bringing the reaction mixture to high temperature water (HTW) conditions and/or by mixing the aqueous reaction mixture with a solid catalyst, such as for example a smectite clay. The present invention further relates to the use of the process of the invention for manufacturing ambrafuran, especially (-)-ambrafuran and other cycloether derivatives.

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