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1,5-Pentanedione, 1,5-diphenyl-, bis(phenylhydrazone) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

557785-76-9

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557785-76-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 557785-76-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,5,7,7,8 and 5 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 557785-76:
(8*5)+(7*5)+(6*7)+(5*7)+(4*8)+(3*5)+(2*7)+(1*6)=219
219 % 10 = 9
So 557785-76-9 is a valid CAS Registry Number.

557785-76-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,5-diphenylpentyl-1,5-dione bisphenylhydrazone

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:557785-76-9 SDS

557785-76-9Relevant academic research and scientific papers

Transformations of mono- and bisphenylhydrazones of aliphatic-aromatic 1,5-diketones under the conditions of the fischer reaction

Moskovkina

, p. 1190 - 1199 (2007/10/03)

The mono- and bisphenylhydrazones of 3-R-1,5-diphenylpentane-1,5-diones were obtained, and their transformations in the Fischer indole synthesis under various conditions were studied. It was shown that 4-R-2,6-diphenylpyridines, 2-phenylindole, and 5-R-1,-3-diphenyl-Δ2-pyrazolines are formed as the main products in addition to the 3-R-1-phenyl-3-(2-phenyl-3-indolyl)propan-1-ones or their phenylhydrazones produced as a result of indolization. The ways of formation of these compounds are discussed. Some transformations of the obtained ketones were studied.

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