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10151-96-9

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10151-96-9 Usage

Description

2-[(4-methylphenyl)amino]-2-oxoethyl thiocyanate is a chemical compound characterized by the molecular formula C10H10N2OS. It is a thiocyanate derivative featuring a substituted phenyl group and a ketone functional group, which contributes to its reactivity and potential applications in various fields.

Uses

Used in Chemical Reactions and Synthesis Processes:
2-[(4-methylphenyl)amino]-2-oxoethyl thiocyanate is utilized as a reagent or intermediate in various chemical reactions and synthesis processes. Its unique structure allows it to participate in a range of organic transformations, facilitating the creation of new compounds with diverse properties.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-[(4-methylphenyl)amino]-2-oxoethyl thiocyanate is used as a building block or precursor for the development of new drugs. Its chemical properties may contribute to the design of innovative therapeutic agents with potential applications in treating various diseases and medical conditions.
Used in Agrochemical Industry:
2-[(4-methylphenyl)amino]-2-oxoethyl thiocyanate may also find applications in the agrochemical industry, where it could be employed as a component in the synthesis of pesticides, herbicides, or other agricultural chemicals. Its chemical structure may offer new possibilities for enhancing the effectiveness and selectivity of these products.
Used in Materials Science:
In the field of materials science, 2-[(4-methylphenyl)amino]-2-oxoethyl thiocyanate could be explored for its potential to contribute to the development of new materials with unique properties. Its incorporation into polymers, coatings, or other materials may lead to advancements in areas such as electronics, textiles, or construction.
Safety Precautions:
It is crucial to handle 2-[(4-methylphenyl)amino]-2-oxoethyl thiocyanate with care and implement appropriate safety measures during its use, storage, and disposal. Due to its potential hazards, it is essential to follow recommended guidelines and protocols to minimize risks to human health and the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 10151-96-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,1,5 and 1 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 10151-96:
(7*1)+(6*0)+(5*1)+(4*5)+(3*1)+(2*9)+(1*6)=59
59 % 10 = 9
So 10151-96-9 is a valid CAS Registry Number.

10151-96-9SDS

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 [2-(4-methylanilino)-2-oxoethyl] thiocyanate

1.2 Other means of identification

Product number -
Other names 2-thiocyanato-N-p-tolyl-acetamide

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:10151-96-9 SDS

10151-96-9Relevant articles and documents

A convenient, rapid, and general synthesis of α-oxo thiocyanates using clay supported ammonium thiocyanate

Meshram,Thakur, Pramod B.,Madhu Babu,Bangade, Vikas M.

experimental part, p. 1780 - 1785 (2012/05/04)

A very rapid, convenient, and general method for the synthesis of α-oxo thiocyanates has been described by using clay supported ammonium thiocyanate. The procedure avoids the use of additional catalyst, solvent, aqueous work-up and the yields are high. Moreover, the method is applicable for a variety of aryl, heteroaryl, alkyl α-halo carbonyls, β-keto tosylates, α-halo β-dicarbonyl, α-tosyl, β-dicarbonyl, alkyl halide, and alkyl tosylates.

Production of carbonyl compounds substituted in α-position

-

, (2008/06/13)

Production of carbonyl compounds substituted in the α-position and having the formula: EQU1 wherein R1 is alkyl, aralkyl, phenyl, toluyl, naphthyl, alkoxy or amino; R2 is hydrogen EQU2 A is hydrogen, alkyl, halo or EQU3 R6 is hydrogen or methyl, and R11 is alkyl; wherein said compounds are formed by reacting a sulfur ylide having the formula: EQU4 wherein Y is the radical EQU5 and R9 and R10 are alkyl or phenyl, with a solution containing both an electrophilic agent A' that is converted into the radical A and a nucleophilic agent B' that is converted into the radical B. The resulting carbonyl compounds are useful as starting materials for the production of paper, textile, and leather auxiliaries, plant protection agents, alkyd resins, polyesters and polyamides.

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