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Benzoic acid, 4-methoxy-2-methyl-6-(phenylmethoxy)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

68048-09-9

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68048-09-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 68048-09-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,0,4 and 8 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 68048-09:
(7*6)+(6*8)+(5*0)+(4*4)+(3*8)+(2*0)+(1*9)=139
139 % 10 = 9
So 68048-09-9 is a valid CAS Registry Number.

68048-09-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-benzyloxy-4-methoxy-6-methylbenzoic acid

1.2 Other means of identification

Product number -
Other names 2-Benzyloxy-4-methoxy-6-methyl-benzoesaeure

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:68048-09-9 SDS

68048-09-9Relevant academic research and scientific papers

Synthesis of Lichen para-Sphaerophorol Depsides

Elix, John A.,Wardlaw, Judith H.

, p. 425 - 429 (2007/10/02)

The total synthesis of the lichen depsides sphaerophorin (1), 4-O-demethylsphaerophorin (2), isosphaeric acid (3), hyperlatolic acid (4) and isohyperlatolic acid (5) is described.

Depsidone Synthesis. Part 16. Benzophenone-Grisa-3',5'-diene-2',3-dione-depsidone Interconversion: a New Theory of Depsidone Biosynthesis

Sala, Tony,Sargent, Melvyn V.

, p. 855 - 869 (2007/10/02)

The synthesis of a number of grisa-3',5'-diene-2',3-diones by oxidative coupling of substituted 2,2'-dihydroxy-4-methoxybenzophenones is described.The rearrangement of these grisadienediones to depsidones under basic, acidic, and thermal conditions is des

Synthesis of Bikaverin

Katagiri, Nobuya,Nakano, Jun,Kato, Tetsuzo

, p. 2710 - 2716 (2007/10/02)

The total synthesis of bikaverin (1b) is described, from everninic acid (5) and 3,5-dihydrobenzoic acid (6).Dieckmann condensation of methyl 2-acetyl-3,5-bis(benzyloxy)phenylacetate (14), synthesised from (6), followed by treatment with protected everninic acid chloride (9) gave 1,3-bisbenzyloxy-6,8-bis(2-benzyloxy-4-methoxy-6-methylbenzyloxy)naphthalene (16).Photoinduced Fries rearrangement of (16) afforded 1,3-bis(benzyloxy)-7-(2-benzyloxy-4-methoxy-6-methylbenzoyl)-6-(2-benzyloxy-4-methoxy-6-methylbenzoyloxy)-8-hydroxynaphthalene (23).Ring closure of (23) with tetramethylammonium hydroxide in pyridine gave the angular benzoxanthene, 1,3-bis(benzyloxy-6-hydroxy)-10-methoxy-8-methylbenzoxanthen-7-one (25), which was oxidized with potassium dichromate to give the orthoquinone, 1,3-bis(benzyloxy)-10-methoxy-8-methylbenzoxanthen-5,6,7-trione (28).By a novel type of rearrangement, (28) was transformed into the linear benzoxanthen, 8,10-bis(benzyloxy)-3-methoxy-1-methylbenzoxanthen-6,11,12-trione (29) by treatment with silica gel.Oxidation and debenzylation of (29) with manganese dioxide in concentrated H2SO4 gave norbikaverin (1a).

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