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1-butyl-2-methoxy-3-(methoxymethyl)benzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

223578-05-0

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223578-05-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 223578-05-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,3,5,7 and 8 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 223578-05:
(8*2)+(7*2)+(6*3)+(5*5)+(4*7)+(3*8)+(2*0)+(1*5)=130
130 % 10 = 0
So 223578-05-0 is a valid CAS Registry Number.

223578-05-0SDS

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 1-butyl-2-methoxy-3-(methoxymethyl)benzene

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:223578-05-0 SDS

223578-05-0Upstream product

223578-05-0Relevant articles and documents

Total synthesis of phomazarin

Boger, Dale L.,Hong, Jiyong,Hikota, Masataka,Ishida, Michio

, p. 2471 - 2477 (1999)

A concise total synthesis of phomazarin (1) is detailed enlisting a heterocyclic azadiene inverse electron demand Diels-Alder reaction (1,2,4- triazine → pyridine) for preparation of the fully substituted and appropriately functionalized pyridine C-ring. Thus, [4 + 2] cycloaddition (85%) of triethyl 1,2,4-triazine3,5,6-tricarboxylate (2) with trimethoxyethylene (3) followed by conversion of the cycloadduct 11 to the cyclic anhydride 13 provided the phomazarin C-ring with the three carboxylates suitably differentiated. Linkage of the A- and C-rings through selective nucleophilic addition of the aryllithium reagent 9 to the least hindered anhydride carbonyl of 13 followed by Friedel-Crafts closure of the B-ring provided the fully functionalized phomazarin skeleton. The successful structural correlation of synthetic 1 with natural material and its derivatives confirmed the latest structural assignment for the natural product.

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