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142605-85-4

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142605-85-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 142605-85-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,2,6,0 and 5 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 142605-85:
(8*1)+(7*4)+(6*2)+(5*6)+(4*0)+(3*5)+(2*8)+(1*5)=114
114 % 10 = 4
So 142605-85-4 is a valid CAS Registry Number.

142605-85-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 6,6-bis(4-chlorophenyl)-3-methyl-1,2-dioxan-3-ol

1.2 Other means of identification

Product number -
Other names -

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:142605-85-4 SDS

142605-85-4Relevant articles and documents

Manganese(II and III)-Mediated Synthesis of Cyclic Peroxides from Alkenes, Active Methylene Compounds, and Molecular Oxygen

Qian, Chang-Yi,Yamada, Takashi,Nishino, Hiroshi,Kurosawa, Kazu

, p. 1371 - 1378 (2007/10/02)

The reaction of 1,1-diphenylethene, 1,1-bis(4-chlorophenyl)ethene, 1,1-bis(4-methylphenyl)ethene, 1,1-bis(4-methoxyphenyl)ethene, and 1,1-bis(4-fluorophenyl)ethene with 2-methyl-1,3-cyclohexanedione, 2-methyl-1,3-cyclopentanedione, 2-acetylcyclohexanone, ethyl 2-acetyl-3-oxobutanoate, 3-methyl-2,4-pentanedione, 1,3-cyclohexanedione, and 2,4-pentanedione in the presence of Mn(OAc)2 and molecular oxygen yielded the corresponding cyclic peroxides in moderate-to-good yields.Similar reaction of 1,1-disubstituted alkenes with 1,3-cyclopentanedione in the presence of Mn(OAc)3 and molecular oxygen gave 2,2,9,9-tetraphenyloctahydro-3,4,7,8-tetraoxabenzindene-4a,6a-diols.Acid-catalyzed decomposition of 4-acetyl-6,6-diaryl-3-methyl-1,2-dioxan-3-ols yielded 3-acetyl-5-aryl-2-methylfurans in moderate yields.Treatment of the 4-acetyl-6,6-diaryl-3-methyl-1,2-dioxan-3-ols with alkali gave 6,6-diaryl-3-methyl-1,2-dioxan-3-ols which gave 1-aryl-1,4-pentanediones upon treatment with hydrochloric acid in acetic acid.The synthetic utility and mechanism of the reactions are discussed.

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