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4111-08-4

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4111-08-4 Usage

Description

2-Hydroxy-2-methylbutanenitrile, also known as a cyanohydrin, is an organic compound characterized by the presence of a hydroxyl group and a nitrile group on the alpha carbon. It has ethyl and methyl substituents on the alpha carbon, making it a unique and versatile molecule. This colorless oil exhibits distinct chemical properties that make it suitable for various applications across different industries.

Uses

Used in Chemical Synthesis:
2-Hydroxy-2-methylbutanenitrile is used as an intermediate in the chemical synthesis of various compounds, particularly in the pharmaceutical and agrochemical industries. Its unique structure allows for the creation of a wide range of derivatives, making it a valuable building block for the development of new molecules with potential applications in these fields.
Used in Flavor and Fragrance Industry:
2-Hydroxy-2-methylbutanenitrile is used as a building block for the synthesis of various flavor and fragrance compounds. Its unique chemical structure contributes to the creation of novel scents and flavors, enhancing the sensory experience in the perfumery and food industries.
Used in Polymer Industry:
In the polymer industry, 2-hydroxy-2-methylbutanenitrile is used as a monomer for the production of specialty polymers with specific properties. Its incorporation into polymer chains can lead to materials with enhanced mechanical, thermal, or chemical resistance, depending on the desired application.
Used in Pharmaceutical Industry:
2-Hydroxy-2-methylbutanenitrile is used as a starting material for the synthesis of various pharmaceutical compounds, including drugs with potential therapeutic applications. Its unique structure allows for the development of new drugs with improved efficacy and reduced side effects.
Used in Agrochemical Industry:
In the agrochemical industry, 2-hydroxy-2-methylbutanenitrile is used as a precursor for the synthesis of various agrochemicals, such as pesticides and herbicides. Its unique chemical properties enable the development of more effective and environmentally friendly products for agricultural use.

Check Digit Verification of cas no

The CAS Registry Mumber 4111-08-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,1,1 and 1 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 4111-08:
(6*4)+(5*1)+(4*1)+(3*1)+(2*0)+(1*8)=44
44 % 10 = 4
So 4111-08-4 is a valid CAS Registry Number.
InChI:InChI=1/C5H9NO/c1-3-5(2,7)4-6/h7H,3H2,1-2H3

4111-08-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-hydroxy-2-methylbutanenitrile

1.2 Other means of identification

Product number -
Other names methylethylketone cyanhydrine

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:4111-08-4 SDS

4111-08-4Relevant articles and documents

Kirby et al.

, p. 53,59 (1968)

Catalytic Transfer Hydration of Cyanohydrins to α-Hydroxyamides

Kanda, Tomoya,Naraoka, Asuka,Naka, Hiroshi

supporting information, p. 825 - 830 (2019/01/14)

We report the palladium(II)-catalyzed transfer hydration of cyanohydrins to α-hydroxyamides by using carboxamides as water donors. This method enables selective hydration of various aldehyde- and ketone-derived cyanohydrins to afford α-mono- and α,α-disubstituted-α-hydroxyamides, respectively, under mild conditions (50 °C, 10 min). The direct conversion of fenofibrate, a drug bearing a benzophenone moiety, into a functionalized α,α-diaryl-α-hydroxyamide was achieved by means of a hydrocyanation-transfer hydration sequence. Preliminary kinetic studies and the synthesis of a site-specifically 18O-labeled α-hydroxyamide demonstrated the carbonyl oxygen transfer from the carboxamide reagent into the α-hydroxyamide product.

BIOFILM CONTROL

-

Page/Page column 9, (2008/06/13)

Compositions and methods suitable for killing bacteria and controlling biofilms comprising one or more microorganisms are provided wherein molecules capable of emulating cell-to-cell signal molecules of the microorganisms are utilized.

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