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2-pentanone, 2-(1-methylbutylidene)hydrazone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

34912-38-4

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34912-38-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 34912-38-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,9,1 and 2 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 34912-38:
(7*3)+(6*4)+(5*9)+(4*1)+(3*2)+(2*3)+(1*8)=114
114 % 10 = 4
So 34912-38-4 is a valid CAS Registry Number.

34912-38-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name bis-(1-methyl-butylidene)-hydrazine

1.2 Other means of identification

Product number -
Other names pentan-2-one azine

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:34912-38-4 SDS

34912-38-4Relevant academic research and scientific papers

Process for preparing ketazine by molecular oxygen oxidation method

-

Paragraph 0056-0057, (2019/07/04)

The invention discloses a process for preparing ketazine by a molecular oxygen oxidation method, which comprises the following steps: ketimine is prepared, and ketone and ammonia are put into a pressure kettle according to a ratio;a pressure range is adjusted to be1.0-5.0MPa, a temperature range to be30-180 DEG C, and a reaction time to be 3-5 hours to generate the ketimine; the molar ratio of theammonia to the ketone is 1:1-20:1; the temperature and the pressure are reduced, and a mixture of the ketimine and the ketone is separated; the mixture of the ketimine and the ketone, a catalyst anda drying agent are put into a reaction kettle and heated to 30-80 DEG C, molecular oxygen is introduced to perform oxidation reaction, wherein the pressure range is 0-1.0MPa, and the reaction time is3-6 hours, and molecular oxygen included: oxygen or air; ketazine is separated and purified.The method is not only suitable for benzophenone, but also achieves theketazine of aliphatic ketone with fewcarbon atoms. The method has wide source of raw materials, low cost and easy recovery, no saline wastewater, low energy consumption and cost, and is environmentally friendly.

Ruthenium(ii)-catalysed direct synthesis of ketazines using secondary alcohols

Kishore, Jugal,Thiyagarajan, Subramanian,Gunanathan, Chidambaram

supporting information, p. 4542 - 4545 (2019/04/26)

Direct one-pot synthesis of ketazines from secondary alcohols and hydrazine hydrate catalyzed by a ruthenium pincer complex is reported, which proceeds through O-H bond activation of secondary alcohols via amine-amide metal-ligand cooperation in the catalyst. Remarkably, liberated molecular hydrogen and water are the only byproducts.

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