6749-93-5 Usage
Description
Cyclopropylmethyl 4-nitrobenzoate is a chemical compound with the molecular formula C11H11NO4. It is a yellow crystalline solid that is insoluble in water but soluble in organic solvents. The cyclopropylmethyl group in the molecule provides stability and enhanced reactivity, making it a valuable component in the production of a wide range of chemical products.
Uses
Used in Pharmaceutical Industry:
Cyclopropylmethyl 4-nitrobenzoate is used as an intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of various biologically active compounds.
Used in Agrochemical Industry:
Cyclopropylmethyl 4-nitrobenzoate is used as an intermediate in the synthesis of agrochemicals, playing a role in the creation of substances that can help control, prevent, or kill pests in agriculture.
Used in Organic Chemistry:
Cyclopropylmethyl 4-nitrobenzoate is used as a building block in organic chemistry, particularly in the synthesis of various biologically active compounds, due to its stability and enhanced reactivity.
Check Digit Verification of cas no
The CAS Registry Mumber 6749-93-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,7,4 and 9 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6749-93:
(6*6)+(5*7)+(4*4)+(3*9)+(2*9)+(1*3)=135
135 % 10 = 5
So 6749-93-5 is a valid CAS Registry Number.
6749-93-5Relevant articles and documents
Aerobic oxidative esterification and thioesterification of aldehydes using dibromoisocyanuric acid under mild conditions: No metal catalysts required
Kwon, Young-Do,La, Minh Thanh,Kim, Hee-Kwon
, p. 10833 - 10841 (2018/07/05)
A practical direct method for the direct preparation of esters and thioesters from aldehydes is described. Esters and thioesters were synthesized by oxidative esterification and thioesterification via in situ generated acyl bromide intermediates, which were used to react with various alcohols and thiols. The esterification and thioesterification were readily performed in the presence of dibromoisocyanuric acid in dichloromethane, without any metal catalysts and under mild conditions. By using this reaction protocol, various esters and thioesters were prepared in high yields. This effective method offers a promising approach for the facile esterification and thioesterification of aldehydes.
