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190774-56-2

190774-56-2

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190774-56-2 Usage

Chemical Properties

clear yellow liquid

Check Digit Verification of cas no

The CAS Registry Mumber 190774-56-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,0,7,7 and 4 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 190774-56:
(8*1)+(7*9)+(6*0)+(5*7)+(4*7)+(3*4)+(2*5)+(1*6)=162
162 % 10 = 2
So 190774-56-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H9NOS/c1-7-3-4-9(11-2)8(5-7)10-6-12/h3-5H,1-2H3

190774-56-2 Well-known Company Product Price

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  • (Code)Product description
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  • Alfa Aesar

  • (L11085)  2-Methoxy-5-methylphenyl isothiocyanate, 99%   

  • 190774-56-2

  • 1g

  • 308.0CNY

  • Detail

  • Alfa Aesar

  • (L11085)  2-Methoxy-5-methylphenyl isothiocyanate, 99%   

  • 190774-56-2

  • 5g

  • 1019.0CNY

  • Detail

  • Aldrich

  • (474967)  2-Methoxy-5-methylphenylisothiocyanate  98%

  • 190774-56-2

  • 474967-2G

  • 973.44CNY

  • Detail

190774-56-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-isothiocyanato-1-methoxy-4-methylbenzene

1.2 Other means of identification

Product number -
Other names 2-Methoxy-5-methylphenyl isothiocyanate

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:190774-56-2 SDS

190774-56-2Upstream product

190774-56-2Relevant articles and documents

Synthesis of Isothiocyanates and Unsymmetrical Thioureas with the Bench-Stable Solid Reagent (Me4N)SCF3

Scattolin, Thomas,Klein, Alexander,Schoenebeck, Franziska

supporting information, p. 1831 - 1833 (2017/04/11)

A highly efficient, selective, and rapid transformation of primary amines and diamines to isothiocyanates and cyclic thioureas is disclosed. As opposed to established approaches that employ toxic or volatile electrophilic liquids and require reaction control (i.e., slow addition, cooling), this protocol utilizes the bench-stable, solid reagent (Me4N)SCF3 at room temperature. The method is characterized by operational simplicity, high speed, efficiency, high functional group tolerance, and late-stage applicability. The byproducts are solids, allowing isolation of the target compounds by filtration.

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