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Heptanal, phenylhydrazone is a chemical compound with the molecular formula C13H19N. It is formed by the reaction of heptanal, a seven-carbon aldehyde, with phenylhydrazine, an aromatic amine. Heptanal, phenylhydrazone is an example of a hydrazone, which is a derivative of a carbonyl compound (such as an aldehyde or ketone) where the carbonyl group has been replaced by a hydrazone group. Heptanal, phenylhydrazone is often used in organic synthesis and as an analytical reagent. It is a pale yellow solid that is soluble in organic solvents and has a characteristic odor. The compound is also known for its use in the detection of aldehydes and ketones, as it forms colored complexes with these functional groups, which can be useful in qualitative analysis.

6228-45-1

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6228-45-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6228-45-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,2 and 8 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6228-45:
(6*6)+(5*2)+(4*2)+(3*8)+(2*4)+(1*5)=91
91 % 10 = 1
So 6228-45-1 is a valid CAS Registry Number.

6228-45-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name heptanal phenylhydrazone

1.2 Other means of identification

Product number -
Other names Oenanthyliden-phenylhydrazin

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:6228-45-1 SDS

6228-45-1Relevant academic research and scientific papers

Visible light-mediated C-H difluoromethylation of electron-rich heteroarenes

Su, Yi-Ming,Hou, Yu,Yin, Feng,Xu, Yue-Ming,Li, Yan,Zheng, Xiaoqi,Wang, Xi-Sheng

supporting information, p. 2958 - 2961 (2014/06/23)

A novel method for visible-light photoredox-catalyzed difluoromethylation of electron-rich N-, O-, and S-containingheteroarenes under mild reaction conditions is developed. Mechanistic investigation indicates that the net C-H difluoromethylation proceeds through an electrophilic radical-type pathway.

Novel derivatives of 3-alkyl-1,5-diaryl-1H-1,2,4-triazoles and their pharmacological evaluation as CB1 cannabinoid ligands

Hernandez-Folgado, Laura,Goya, Pilar,Frigola, Jordi,Cuberes, Maria Rosa,Dordal, Alberto,Holenz, Joerg,Jagerovic, Nadine

experimental part, p. 1073 - 1082 (2009/10/24)

In a previous study, we have identified 3-alkyl-1,5-diaryl-1H-1,2,4- triazoles to be a novel class of cannabinoid type-1 (CB1) receptor antagonists. However, the synthesis yields for the ligands were low. Here we present an alternative synthesi

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