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6794-04-3

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6794-04-3 Usage

Chemical compound

2-[2-(benzyloxy)ethoxy]ethyl acetate

Physical properties

clear, colorless liquid with a faint odor

Uses

solvent, chemical intermediate

Synthesis method

reaction between benzyloxyethanol and ethylene oxide, followed by esterification with acetic acid

Toxicity

low acute toxicity

Environmental impact

not harmful

Primary use

solvent in industrial applications like paint and coating formulations

Additional use

fragrance ingredient in consumer products

Check Digit Verification of cas no

The CAS Registry Mumber 6794-04-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,7,9 and 4 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6794-04:
(6*6)+(5*7)+(4*9)+(3*4)+(2*0)+(1*4)=123
123 % 10 = 3
So 6794-04-3 is a valid CAS Registry Number.

6794-04-3SDS

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 2-(2-phenylmethoxyethoxy)ethyl acetate

1.2 Other means of identification

Product number -
Other names 2-Acetoxy-2'-benzyloxy-diethylether

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:6794-04-3 SDS

6794-04-3Upstream product

6794-04-3Downstream Products

6794-04-3Relevant articles and documents

A One-step and Chemoselective Conversion of Silyl-protected Alcohols into the Corresponding Acetates

Oriyama, Takeshi,Oda, Mihoko,Gono, Junko,Koga, Gen

, p. 2027 - 2030 (2007/10/02)

A reagent system of acetyl bromide combined with a catalytic amount of tin(II) bromide cleaves readily trialkylsilyl ethers to give the corresponding acetates in high yields under very mild conditions.

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