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Benzeneacetaldehyde, a-ethyl-a-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

105539-07-9

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105539-07-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 105539-07-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,5,3 and 9 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 105539-07:
(8*1)+(7*0)+(6*5)+(5*5)+(4*3)+(3*9)+(2*0)+(1*7)=109
109 % 10 = 9
So 105539-07-9 is a valid CAS Registry Number.

105539-07-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2-diphenyl-butyraldehyde

1.2 Other means of identification

Product number -
Other names 2,2-Diphenyl-butyraldehyd

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:105539-07-9 SDS

105539-07-9Relevant academic research and scientific papers

α-hydrdroxylic acid derivatives, their production and use

-

Page column 18-19, (2010/11/30)

The present invention relates to carboxylic acid derivatives of the formula where the radicals have the meanings stated in the description, to the preparation of these compounds and to their use as drugs.

Reactions of a β-sultam ring with Lewis acids via the C-S bond cleavage

Iwama, Tetsuo,Ogawa, Miyoko,Kataoka, Tadashi,Muraoka, Osamu,Tanabe, Genzoh

, p. 8941 - 8974 (2007/10/03)

Selective C-S bond cleavage of a β-sultam ring was achieved by the reactions with Lewis acids. Aryl ketones or aldehyde were provided from 3- aryl-β-sultams whereas β-sultams bearing a poorly migratory substituent at C-3 gave trans-1,2,3-oxathiazolidine 2-oxides and/or cis-aziridines. These reactions were influenced by the cation-stabilizing capability of C-4 substituents and by the configuration of the substituents at C-3 and C-4. Some 4-alkenyl-3-aryl-β-sultams underwent tandem intramolecular cyclization to give bicyclo[3.2.1]- and [2.2.1]-γ-sultams via the processes of C-S bond cleavage, 1,2-aryl shift, cation-olefin cyclization and recombination of the sulfonyl anion.

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