6861-53-6

Basic information

• Product Name: Benzene, 1,1'-(dimethoxymethylene)bis[4-chloro-
• CAS NO: 6861-53-6
• Molecular Formula: C15H14Cl2O2
• Molecular Weight: 297.181
• Mol File: 6861-53-6.mol
• Article Data: 12

Chemical Properties

• CAS DataBase Reference: Benzene, 1,1'-(dimethoxymethylene)bis[4-chloro-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1,1'-(dimethoxymethylene)bis[4-chloro-(6861-53-6)
• EPA Substance Registry System: Benzene, 1,1'-(dimethoxymethylene)bis[4-chloro-(6861-53-6)

Safety Data

• Hazardous Substances Data: 6861-53-6(Hazardous Substances Data)

Upstream product

• 67-56-1 methanol 
• 21367-49-7 4,4'-dichloro-benzophenone 4-phenyl-semicarbazone 
• 104-15-4 toluene-4-sulfonic acid 
• 90-98-2 4,4'-Dichlorobenzophenone 
• 149-73-5 trimethyl orthoformate 
• 7457-25-2 bis-(4-chlorophenyl)-dichloromethane 
• 124-41-4 sodium methylate 
• 5463-11-6 4,4'-dichlorobenzophenone hydrazone 

Downstream Products

• 1296664-72-6 2,2-bis(4-chloro phenyl)-5-methyl-1,3-dioxane-5-carboxylic acid 
• 1296664-73-7 C₆₉H₉₃Cl₂NO₁₆ 
• 1296664-95-3 C₂₅H₁₇Cl₅O₅ 
• 161368-10-1 Methyl (2,2-di[4-chlorophenyl]-1,3-benzodioxolan-5-yl)acetate 

Relevant articles and documents

Highly efficient acetalization of carbonyl compounds catalyzed by anilin-aldehyde resin salts

A mild procedures for the syntheses of ethylene acetals and dimethyl acetals from the corresponding aldehydes and ketones catalyzed by 1mol% of anilinealdehyde resin salts are described. This method is also useful for the synthesis of dimethyl acetals of diaryl ketones.

PROCESS FOR THE PREPARATION OF RAPAMYCIN DERIVATIVES

The invention relates to processes for the preparation of compound of CCI-779 having the Formula (I), which is useful as an antineoplastic agent. The invention further relates to certain novel intermediates useful in the preparation of compound of CCI-779 and processes for their preparation. The invention also relates to pharmaceutical compositions that include the compound of CCI-779, prepared according to the processes disclosed herein.

Iron(III) tosylate in the preparation of dimethyl and diethyl acetals from ketones and β-keto enol ethers from cyclic β-diketones

An efficient method for conversion of ketones to their corresponding dimethyl and diethyl acetals and of cyclic β-diketones into β-keto enol ethers using Fe(OTs)3 as a catalyst is described. Copyright Taylor & Francis Group, LLC.