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2'-METHOXY-3-(3-METHOXYPHENYL)PROPIOPHENONE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

75849-06-8

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75849-06-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 75849-06-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,8,4 and 9 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 75849-06:
(7*7)+(6*5)+(5*8)+(4*4)+(3*9)+(2*0)+(1*6)=168
168 % 10 = 8
So 75849-06-8 is a valid CAS Registry Number.
InChI:InChI=1/C17H18O3/c1-19-14-7-5-6-13(12-14)10-11-16(18)15-8-3-4-9-17(15)20-2/h3-9,12H,10-11H2,1-2H3

75849-06-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2-methoxyphenyl)-3-(3-methoxyphenyl)propan-1-one

1.2 Other means of identification

Product number -
Other names 2'-METHOXY-3-(3-METHOXYPHENYL)PROPIOPHENONE

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:75849-06-8 SDS

75849-06-8Upstream product

75849-06-8Relevant academic research and scientific papers

Intramolecular Alkylation of Phenols. Part 5. A Regiospecific Anionic Ring Closure of Phenols via Quinone Methides

Murphy, William S.,Wattanasin, Sompong

, p. 1567 - 1577 (2007/10/02)

The bis-magnesium salts of the triols (6a) and (6h) cyclise when heated in benzene with high ortho-regiospecificity to the corresponding bis-phenols (7) and (8).The triols (6k) and (6o) under the same conditions cyclise with high para-regiospecificity to the corresponding bis-phenols (7) and (8).Both (6a) and (6h) cyclise via o-quinone methides, and (6k) and (6o) via p-quinone methides.Results from the use of, inter alia, 18-crown-6, indicate that the high ortho-regiospecificity of the cyclisation of (6a) and (6h) is due to intramolecular Mg(II) bridging of the intermediate o-quinone methides.The high para-regiospecificity of cyclisation of (6k) and (6o) is due to steric hindrance towards o-cyclisation of the intermediate p-quinone methides presented by the Mg(II) cation.The unexpected facility with which (6a) and (6k) undergo ring closure is discussed.

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