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Dipentan-3-ylidenehydrazine is a chemical compound with the molecular formula C10H20N2. It is an organic compound that features a hydrazine functional group attached to a dipentan-3-yl moiety, which is a five-carbon chain with a double bond between the third and fourth carbon atoms. dipentan-3-ylidenehydrazine is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, particularly as an intermediate in the production of certain pesticides and drugs. Its structure and reactivity make it a valuable building block in organic chemistry, although it should be handled with care due to its potential toxicity and reactivity with other chemicals.

1530-17-2

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1530-17-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1530-17-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,3 and 0 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1530-17:
(6*1)+(5*5)+(4*3)+(3*0)+(2*1)+(1*7)=52
52 % 10 = 2
So 1530-17-2 is a valid CAS Registry Number.

1530-17-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(pentan-3-ylideneamino)pentan-3-imine

1.2 Other means of identification

Product number -
Other names Bis-(1-aethyl-propyliden)-hydrazin

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:1530-17-2 SDS

1530-17-2Relevant academic research and scientific papers

Synthesis of Ketazines from Dinitrogen Coordinated to Tungsten

Hidai, Masanobu,Kurano, Masa-aki,Mizobe, Yasushi

, p. 2719 - 2720 (1985)

When treated with a methanol/acetone mixture at 50 deg C, the complex trans- gives acetone azine in moderate yield, although the yield is slightly lower than that from cis-.Under UV irradiation, these dinitrogen complexes produce acetone azine even at room temperature.

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.

Azine synthesis via nitrogen-nitrogen bond formation

Love,Tsai

, p. 3101 - 3108 (2007/10/02)

Imine anions, generated by reaction of nitriles with organometallic reagents, are dimerized to form symmetrical azines through the use of CuI and t-butyl peroxybenzoate.

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