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2,6-bis(benzyloxy)-4-methoxyphenyl acetate is a chemical compound characterized by the molecular formula C23H22O5. It is an ester that originates from the reaction of acetic acid with 2,6-bis(benzyloxy)-4-methoxyphenol. This white crystalline solid, with a melting point of 60-63°C, is insoluble in water but readily soluble in organic solvents. Due to its potential to cause irritation to the skin, eyes, and respiratory tract, careful handling is advised. Its versatility in organic chemistry makes it a valuable component in the synthesis of various organic compounds.

6962-64-7

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6962-64-7 Usage

Uses

Used in Organic Synthesis:
2,6-bis(benzyloxy)-4-methoxyphenyl acetate is utilized as a key intermediate in organic synthesis for the preparation of a range of organic compounds. Its unique structure allows it to serve as a building block, facilitating the creation of complex molecules with specific properties.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2,6-bis(benzyloxy)-4-methoxyphenyl acetate is used as a precursor in the synthesis of pharmaceutical agents. Its reactivity and structural features make it suitable for the development of new drugs with potential therapeutic applications.
Used in Chemical Research:
2,6-bis(benzyloxy)-4-methoxyphenyl acetate is also employed in chemical research as a model compound to study various organic reactions and mechanisms. Its predictable reactivity and solubility profile provide researchers with a reliable system for probing the fundamentals of organic chemistry.
Used in Material Science:
In the field of material science, 2,6-bis(benzyloxy)-4-methoxyphenyl acetate may be used as a component in the development of new materials with specific properties, such as polymers with tailored characteristics for use in various industries.
Overall, 2,6-bis(benzyloxy)-4-methoxyphenyl acetate's applications span across multiple disciplines within the chemical and materials sciences, highlighting its importance as a versatile and valuable compound.

Check Digit Verification of cas no

The CAS Registry Mumber 6962-64-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,6 and 2 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6962-64:
(6*6)+(5*9)+(4*6)+(3*2)+(2*6)+(1*4)=127
127 % 10 = 7
So 6962-64-7 is a valid CAS Registry Number.

6962-64-7SDS

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 [4-methoxy-2,6-bis(phenylmethoxy)phenyl] acetate

1.2 Other means of identification

Product number -
Other names 2-acetoxy-1,3-dibenzyloxy-5-methoxybenzene

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:6962-64-7 SDS

6962-64-7Relevant academic research and scientific papers

Synthesis of Some Pterocarpenes obtained from Brya ebenus

Antus, Sandor,Gottsegen, Agnes,Kolonits, Pal,Nagy, Zoltan,Norgadi, Mihaly,Vermes, Borbala

, p. 1389 - 1394 (2007/10/02)

The syntheses of bryacarpenes-1, -2, and -4, benzopyran (3)>, (+/-)-bryaflavan (+/-)-3',6,7-trihydroxy-2',4'-dimethoxyisoflavan

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