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1,5,7,9,11,15-Pentadecanehexol, 3,13-bis[(phenylmethoxy)methoxy]-, (3R,5R,7R,9S,11R,13R)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

609769-12-2

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609769-12-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 609769-12-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,0,9,7,6 and 9 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 609769-12:
(8*6)+(7*0)+(6*9)+(5*7)+(4*6)+(3*9)+(2*1)+(1*2)=192
192 % 10 = 2
So 609769-12-2 is a valid CAS Registry Number.

609769-12-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (1R,5R,7R,9S,11R,13R)-3,13-bis[(benzyloxy)methoxy]pentadecane-1,5,7,9,11,15-hexol

1.2 Other means of identification

Product number -
Other names (3R,5R,7R,9S,11R,13R)-3,13-Bis-benzyloxymethoxy-pentadecane-1,5,7,9,11,15-hexaol

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:609769-12-2 SDS

609769-12-2Relevant academic research and scientific papers

Selective hydrolysis of anti-1,3-diol-acetonides for the differentiation of 1,3-anti and 1,3-syn diols

Coste, Gérald,Gerber-Lemaire, Sandrine

, p. 671 - 674 (2006)

A mild and general method for the selective cleavage of anti-1,3-acetonides has been developed for the differentiation of 1,3-anti and 1,3-syn diols in long chain polyolic fragments. The diluted acidic conditions applied to these systems are compatible wi

New synthetic routes toward polyketide-like macrolides

Coste, Gérald,Gerber-Lemaire, Sandrine

, p. 685 - 688 (2007/10/03)

New pathways toward the synthesis of polyketide-like macrolides have been developed through the functionalization of long chain polyolic fragments readily obtained from 3,3′-methylenebis{[6-(benzyloxy)methoxy]cyclohept-3-en-1- ol} derivatives 6. This synt

An expeditious, non-iterative, and asymmetric synthesis of 3,5,7,9,11,13,15-heptahydroxypentadecanals

Gerber-Lemaire, Sandrine,Vogel, Pierre

, p. 2959 - 2963 (2007/10/03)

Ozonolysis of (1R,1′R,6R,6′R)-3,3′-methylenebis{6-[(benzyloxy) methoxy]cyclohept-3-en-1-ol} followed by the diastereoselective reduction of the resulting β-hydroxy ketone intermediates gives a rapid route to long-chain polyketides bearing unsymmetrical functions at their terminal positions. These can easily be converted into enantiomerically pure long-chain 1,3-polyol fragments. Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2003.

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