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2,2-Dimethylhexanamide, an organic compound with the chemical formula C8H17NO, is a colorless, oily liquid characterized by a faint odor. It is known for its low toxicity and relative stability under normal conditions, which makes it a versatile and useful chemical in various industrial applications.

20923-67-5

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20923-67-5 Usage

Uses

Used in Polymer Production:
2,2-Dimethylhexanamide is used as a monomer in the production of various polymers, such as nylon and polyurethane. Its chemical properties contribute to the formation of these polymers, enhancing their structural integrity and performance.
Used in Solvent Applications:
As a solvent, 2,2-dimethylhexanamide is employed in various industrial processes to dissolve and mix substances, facilitating chemical reactions and material processing.
Used as a Chemical Intermediate:
2,2-Dimethylhexanamide serves as a chemical intermediate in the synthesis of other organic compounds, playing a crucial role in the production of a wide range of chemical products. Its versatility in chemical reactions makes it an essential component in the manufacturing of various chemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 20923-67-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,9,2 and 3 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 20923-67:
(7*2)+(6*0)+(5*9)+(4*2)+(3*3)+(2*6)+(1*7)=95
95 % 10 = 5
So 20923-67-5 is a valid CAS Registry Number.

20923-67-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2-dimethylhexanamide

1.2 Other means of identification

Product number -
Other names 2,2-dimethyl-hexanoic acid amide

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:20923-67-5 SDS

20923-67-5Relevant academic research and scientific papers

Hypervalent iodine catalyzed hofmann rearrangement of carboxamides using oxone as terminal oxidant

Yoshimura, Akira,Middleton, Kyle R.,Luedtke, Matthew W.,Zhu, Chenjie,Zhdankin, Viktor V.

, p. 11399 - 11404 (2013/02/23)

Hofmann rearrangement of carboxamides to carbamates using Oxone as an oxidant can be efficiently catalyzed by iodobenzene. This reaction involves hypervalent iodine species generated in situ from catalytic amount of PhI and Oxone in the presence of 1,1,1,3,3,3-hexafluoroisopropanol (HFIP) in aqueous methanol solutions. Under these conditions, Hofmann rearrangement of various carboxamides affords corresponding carbamates in high yields.

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