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2-{4-benzyloxy-3-[2,6-dibromo-4-(2,2-dimethyl-[1,3]dioxolan-4-ylmethyl)-phenoxy]-benzylidene}-malonic acid dimethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

845784-36-3

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845784-36-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 845784-36-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,5,7,8 and 4 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 845784-36:
(8*8)+(7*4)+(6*5)+(5*7)+(4*8)+(3*4)+(2*3)+(1*6)=213
213 % 10 = 3
So 845784-36-3 is a valid CAS Registry Number.

845784-36-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name dimethyl 2-(4-(benzyloxy)-3-(2,6-dibromo-4-((2,2-dimethyl-1,3-dioxolan-4-yl)methyl)phenoxy)benzylidene)malonate

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:845784-36-3 SDS

845784-36-3Downstream Products

845784-36-3Relevant academic research and scientific papers

A general method for the synthesis of bastaranes and isobastaranes: First total synthesis of bastadins 5, 10, 12, 16, 20, and 21

Couladouros, Elias A.,Pitsinos, Emmanuel N.,Moutsos, Vassilios I.,Sarakinos, Georgios

, p. 406 - 421 (2007/10/03)

A general strategy for the synthesis of twenty naturally occurring bastadins (all but bastadin 3) is presented. A key retrosynthetic disconnection of the two amide bonds, common in all target molecules, bisects the macrocyclic core into two diaryl ether f

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