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Benzene,1,1'-[(decyloxy)methylene]bis- (9CI), also known as 1,1'-(Decyloxy)methylenebisbenzene or Bis(4-decylphenyl) Ether, is an organic compound with the chemical formula C26H42O2. It is a colorless liquid at room temperature and is characterized by its symmetrical structure, featuring two benzene rings connected by a methylene bridge and two decyloxy groups attached to the benzene rings. Benzene,1,1'-[(decyloxy)methylene]bis- (9CI) is primarily used as a plasticizer, a substance added to plastics to increase their flexibility and workability. It is also employed as a solvent and a chemical intermediate in the synthesis of various organic compounds. Due to its chemical structure, it exhibits low volatility and high boiling point, making it suitable for applications requiring a stable plasticizing agent.

6337-55-9

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6337-55-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6337-55-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,3 and 7 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6337-55:
(6*6)+(5*3)+(4*3)+(3*7)+(2*5)+(1*5)=99
99 % 10 = 9
So 6337-55-9 is a valid CAS Registry Number.

6337-55-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name [decoxy(phenyl)methyl]benzene

1.2 Other means of identification

Product number -
Other names Benzhydryldecylaether

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:6337-55-9 SDS

6337-55-9Downstream Products

6337-55-9Relevant academic research and scientific papers

FeCl3-catalyzed self-cleaving deprotection of methoxyphenylmethyl-protected alcohols

Sawama, Yoshinari,Masuda, Masahiro,Asai, Shota,Goto, Ryota,Nagata, Saori,Nishimura, Shumma,Monguchi, Yasunari,Sajiki, Hironao

supporting information, p. 434 - 437 (2015/03/03)

4-Methoxyphenylmethyl ethers are widely utilized as alcohol protecting groups. FeCl3 effectively catalyzes the deprotection of methoxyphenylmethyl-type ethers in a self-cleaving manner to produce oligomeric derivatives and alcohols. Remarkably, the highly pure mother alcohols can be obtained without silica gel column chromatography by using the 2,4-dimethoxyphenylmethyl group as a protective group.

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