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53088-81-6

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53088-81-6 Usage

Physical state

Colorless, clear liquid

Odor

Floral scent

Uses

a. Solvent
b. Organic synthesis
c. Pharmaceutical industry
d. Perfumes
e. Flavorings
f. Intermediate in the production of plasticizers and surfactants
g. Potential renewable fuel source

Energy content

High

Volatility

Low

Safety precautions

a. Harmful if swallowed or inhaled
b. May cause skin and eye irritation
c. Handle with care

Check Digit Verification of cas no

The CAS Registry Mumber 53088-81-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,0,8 and 8 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 53088-81:
(7*5)+(6*3)+(5*0)+(4*8)+(3*8)+(2*8)+(1*1)=126
126 % 10 = 6
So 53088-81-6 is a valid CAS Registry Number.

53088-81-6SDS

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 3-phenylmethoxypropoxymethylbenzene

1.2 Other means of identification

Product number -
Other names Propan-1,3-dioldibenzylether

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:53088-81-6 SDS

53088-81-6Downstream Products

53088-81-6Relevant articles and documents

Novel Ammonium Ionophores Based on Glycol Dibenzyl Ethers for an Ion-Selective Electrode

Siswanta, Dwi,Hisamoto, Hideaki,Tohma, Hajime,Yamamoto, Noriko,Suzuki, Koji

, p. 945 - 948 (1994)

Based on the finding that dibenzyl ether (DBE) exhibited a relatively high selectively for ammonium ion relative to potassium ion, four types of dibenzyl ethers were synthesized and their ammonium ion selectivities over alkali and alkali-earth metal ions

Intramolecular benzyl-benzyl interactions in protonated benzyl diethers in the gas phase. Effects of internal hydrogen bonding

Edelson-Averbukh, Marina,Etinger, Alexander,Mandelbaum, Asher

, p. 1095 - 1105 (2007/10/03)

Protonated molecules of a variety of benzyl diethers, produced by chemical ionization (CI), undergo a unique rearrangement yielding relatively abundant mlz 181 C14H13+ ions, both in the ion source and under collision-induc

Monobenzylation of 1,n-diols via dibutylstannylene intermediates

Mash, Eugene A.,Kantor, Liza T. A.,Waller, Stephen C.

, p. 507 - 514 (2007/10/03)

Symmetrical primary 1,n-diols, HO(CH2)(n)OH, of any chain length from n = 2-10, can be selectively monobenzylated via sequential treatment with dibutyltin oxide and benzyl bromide.

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