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1016-20-2

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1016-20-2 Usage

Chemical class

Indazole class of organic compounds

Explanation

It belongs to a group of organic compounds that have an indazole ring structure.

Explanation

The presence of different elements in the ring structure differentiates it from other organic compounds.

Explanation

The presence of chlorine atom in the molecule makes it a chlorinated compound, which can affect its reactivity and properties.

Explanation

It serves as a starting material or building block for the synthesis of more complex molecules, particularly in the production of pharmaceuticals and agrochemicals.

Explanation

Due to its unique structure and properties, it may have potential uses in the synthesis of various organic compounds and in the development of new drugs.

Explanation

The properties and uses of this compound can change based on the specific requirements and conditions of its application in different fields.

Explanation

The molecular structure consists of an indazole ring with a butyl group at the 1-position and a chlorine atom at the 5-position, along with a 1,2-dihydro substitution.

Explanation

The solubility of this compound can be influenced by the choice of solvent, which can affect its reactivity and stability in different chemical reactions.

Explanation

The stability of this compound can be affected by various factors, which may impact its shelf life and performance in different applications.

Explanation

As with any chemical compound, it is essential to follow safety guidelines and protocols to minimize the risk of accidents or exposure to harmful substances.

Heterocyclic compound

Contains at least two different elements within its ring structure

Chlorinated compound

Presence of chlorine in its molecular structure

Synthetic intermediate

Used in research and development laboratories

Potential applications

Organic synthesis and medicinal chemistry

Specific characteristics

Vary depending on the context of its application

Molecular structure

1-butyl-5-chloro-1,2-dihydro-3H-indazol-3-one

Solubility

May vary depending on the solvent used

Stability

Can be influenced by factors such as temperature, pH, and exposure to light

Safety precautions

Handle with care and follow proper safety protocols

Check Digit Verification of cas no

The CAS Registry Mumber 1016-20-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,1 and 6 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1016-20:
(6*1)+(5*0)+(4*1)+(3*6)+(2*2)+(1*0)=32
32 % 10 = 2
So 1016-20-2 is a valid CAS Registry Number.

1016-20-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-butyl-5-chloro-1,2-dihydro-indazol-3-one

1.2 Other means of identification

Product number -
Other names 1-Butyl-5-chloro-1,2-dihydro-indazol-3-one

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:1016-20-2 SDS

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