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5-bromo-6-(1,3-dioxan-2-yl)-1,3-benzodioxole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

86449-40-3

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86449-40-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86449-40-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,4,4 and 9 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 86449-40:
(7*8)+(6*6)+(5*4)+(4*4)+(3*9)+(2*4)+(1*0)=163
163 % 10 = 3
So 86449-40-3 is a valid CAS Registry Number.

86449-40-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-bromo-6-(1,3-dioxan-2-yl)-1,3-benzodioxole

1.2 Other means of identification

Product number -
Other names 1-<1-(2-bromo-4,5-methylenedioxyphenyl)>-1,3-dioxane

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:86449-40-3 SDS

86449-40-3Downstream Products

86449-40-3Relevant academic research and scientific papers

Synthesis and optoelectronic properties of hexahydroxylated 10-O-R-substituted anthracenes via a new modification of the friedel-crafts reaction using o-protected ortho-acetal diarylmethanols

Bodzioch, Agnieszka,Marciniak, Bernard,Rozycka-Sokolowska, Ewa,Jeszka, Jeremiasz K.,Uznanski, Pawel,Kania, Sylwester,Kulinski, Janusz,Balczewski, Piotr

scheme or table, p. 4866 - 4876 (2012/05/20)

A new modification of the Friedel-Crafts type intramolecular cyclization involving O-protected ortho-acetal diarylmethanols as a new type of reactant, was carried out for the first time in a medium containing a large amount of water at room temperature an

A synthetic route to highly substituted 1,2,3,4-tetrahydroisoquinolines via Yb(OTf)3-catalyzed diastereoselective ring opening of bridged oxazolidines: Asymmetric synthesis of 2-azapodophyllotoxin

Srivastava, Ajay Kumar,Koh, Minseob,Park, Seung Bum

supporting information; experimental part, p. 4905 - 4913 (2011/06/10)

We herein report a robust and efficient synthetic route to highly functionalized enantiopure 1,2,3,4-tetrahydroisoquinolines (THIQs) from Garner aldehyde. We utilized the inherent chirality of Garner aldehyde through 1,2- and 1,3-/1,4-asymmetric inductions iteratively to obtain 1,2,3,4-tetrasubstitued THIQs using rigid and isolable bridged oxazolidines without any external chiral sources. All possible stereoisomers of bridged oxazoliodines were efficiently synthesized from L- and D-Garner aldehydes and transformed into fully functionalized THIQs via diastereoselective ring opening with various nucleophiles in the presence of Yb(OTf)3. This methodology furnished four out of eight possible diastereomers of 1,2,3,4-tetrasubstituted THIQs despite the electronic nature of substituents on the aryl rings. Finally, the enantioselective synthesis of 2-azapodophyllotoxin was achieved with an overall yield of 35.4 % (eight steps) from D-Garner aldehyde using this synthetic route. A concise and efficient synthetic route to highly functionalized enantiopure 1,2,3,4-tetrahydroisoquinolines (THIQs) from the Garner aldehyde via Yb(OTf)3-catalyzed diastereoselective ring opening of bridged oxazolidines is reported. This methodology was successfully applied to the synthesis of four stereoisomers of THIQ and the enantioselective total synthesis of 2-azapodophyllotoxin (1) in eight steps from D-Garner aldehyde in an overall yield of 35.4 %. Copyright

First asymmetric synthesis of (Un)saturated 1-Alkylbenzo[c]azepin-3-ones: Extension to the corresponding benzazeplnes

Dumoulin, David,Lebrun, Stepfaane,Deniau, Eric,Couture, Axel,Grandclaudon, Pierre

scheme or table, p. 3741 - 3752 (2009/12/05)

A flexible route for the stereoselective synthesis of a variety of structurally diverse (1R)-1-alkyldihydro and tetrahydro-benzazepin(ones) has been developed. The key step is a highly diastereoselective 1,2-addition process applied to a stereopure aromatic hydrazone combined with a ring-closing metathesis reaction to secure the formation of the seven-membered azaheterocycle ring system.

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