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59670-14-3

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59670-14-3 Usage

Physical state

Yellow crystalline solid

Classification

Organic compound, hydrazine derivative

Uses

Reagent in organic synthesis, starting material for pharmaceuticals and agrochemicals production

Biological and pharmacological properties

Potential as an antitumor agent

Pest control properties

Exhibits insecticidal and fungicidal properties

Industrial applications

Versatile and valuable compound in various industries

Check Digit Verification of cas no

The CAS Registry Mumber 59670-14-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,6,7 and 0 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 59670-14:
(7*5)+(6*9)+(5*6)+(4*7)+(3*0)+(2*1)+(1*4)=153
153 % 10 = 3
So 59670-14-3 is a valid CAS Registry Number.

59670-14-3SDS

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 N-methyl-N-[(Z)-(3-methylphenyl)methylideneamino]aniline

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:59670-14-3 SDS

59670-14-3Downstream Products

59670-14-3Relevant articles and documents

A Single Electron Transfer (SET) Approach to C-H Amidation of Hydrazones via Visible-Light Photoredox Catalysis

Zhang, Muliang,Duan, Yingqian,Li, Weipeng,Xu, Pan,Cheng, Jian,Yu, Shouyun,Zhu, Chengjian

, p. 5356 - 5359 (2016/11/02)

The reductive single electron transfer (SET) umpolung amination of aldehyde-derived hydrazones has been developed through visible-light-promoted photoredox catalysis. The ideal transformation of hydrazones into the corresponding hydrazonamide through selective carbon-hydrogen (C-H) bond functionalization represents one of the most step- and atom-economical methods. This SET umpolung strategy features mild conditions and a remarkably broad substrate scope, offering an entirely new substrate class to direct C-H amination.

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