305806-42-2 Usage
Description
METHYL 4-THIAZOL-2-YL-BENZOATE, with the molecular formula C11H9NO2S, is a yellow solid chemical compound that belongs to the class of benzoate esters and thiazole derivatives. It is recognized for its mild, sweet odor and solubility in organic solvents such as ethanol and dichloromethane. METHYL 4-THIAZOL-2-YL-BENZOATE is commonly used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, and also serves as a building block in organic synthesis. Due to its potential hazards and toxicity, it is crucial to handle METHYL 4-THIAZOL-2-YL-BENZOATE with care and follow proper safety protocols.
Uses
Used in Pharmaceutical Industry:
METHYL 4-THIAZOL-2-YL-BENZOATE is used as an intermediate in the synthesis of various pharmaceuticals for its role in creating essential drug components, contributing to the development of new medications.
Used in Agrochemical Industry:
In the agrochemical sector, METHYL 4-THIAZOL-2-YL-BENZOATE is utilized as an intermediate in the production of agrochemicals, playing a part in the formulation of substances that protect crops and enhance agricultural productivity.
Used in Organic Synthesis:
METHYL 4-THIAZOL-2-YL-BENZOATE is used as a building block in organic synthesis for its ability to be incorporated into more complex organic molecules, facilitating the creation of a wide range of chemical products.
Check Digit Verification of cas no
The CAS Registry Mumber 305806-42-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,5,8,0 and 6 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 305806-42:
(8*3)+(7*0)+(6*5)+(5*8)+(4*0)+(3*6)+(2*4)+(1*2)=122
122 % 10 = 2
So 305806-42-2 is a valid CAS Registry Number.
InChI:InChI=1/C11H9NO2S/c1-14-11(13)9-4-2-8(3-5-9)10-12-6-7-15-10/h2-7H,1H3
305806-42-2Relevant articles and documents
Programmed synthesis of arylthiazoles through sequential C-H couplings
Tani, Satoshi,Uehara, Takahiro N.,Yamaguchi, Junichiro,Itami, Kenichiro
, p. 123 - 135 (2014/01/06)
A programmed synthesis of privileged arylthiazoles via sequential C-H couplings catalyzed by palladium or nickel catalysts has been accomplished. This versatile protocol can supply all possible arylthiazole substitution patterns (2-aryl, 4-aryl, 5-aryl, 2
