113772-13-7 Usage
Description
METHYL 2-CYANO-2-(2-NITROPHENYL)ACETATE, with the chemical name Methyl Cyano(2-nitrophenyl)acetate and CAS number 113772-13-7, is a light yellow solid compound that is useful in organic synthesis. It is a versatile intermediate in the synthesis of various organic compounds and has potential applications in different industries.
Uses
Used in Organic Synthesis:
METHYL 2-CYANO-2-(2-NITROPHENYL)ACETATE is used as a synthetic intermediate for the production of various organic compounds. Its unique chemical structure allows it to be a valuable building block in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, METHYL 2-CYANO-2-(2-NITROPHENYL)ACETATE is used as a key intermediate in the synthesis of various drug molecules. Its reactivity and functional groups make it suitable for the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
METHYL 2-CYANO-2-(2-NITROPHENYL)ACETATE is also used in the agrochemical industry as a precursor for the synthesis of various pesticides and insecticides. Its unique properties enable the development of new agrochemicals with improved efficacy and selectivity.
Used in Specialty Chemicals:
In the specialty chemicals sector, METHYL 2-CYANO-2-(2-NITROPHENYL)ACETATE is used as a raw material for the production of various specialty chemicals, such as dyes, pigments, and polymers. Its versatility and reactivity contribute to the development of innovative products with unique properties and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 113772-13-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,7,7 and 2 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 113772-13:
(8*1)+(7*1)+(6*3)+(5*7)+(4*7)+(3*2)+(2*1)+(1*3)=107
107 % 10 = 7
So 113772-13-7 is a valid CAS Registry Number.
InChI:InChI=1/C10H8N2O4/c1-16-10(13)8(6-11)7-4-2-3-5-9(7)12(14)15/h2-5,8H,1H3
113772-13-7Relevant articles and documents
TfOH-Promoted Decyanative Cyclization toward the Synthesis of 2,1-Benzisoxazoles
Zhang, Mengge,Meng, Yonggang,Wu, Yangang,Song, Chuanjun
, p. 7326 - 7332 (2021/06/25)
A novel solvent-free, TfOH-promoted decyanative cyclization approach for the synthesis of 2,1-benzisoxazoles has been developed. The reactions are complete instantly at room temperature and result in the formation of the desired 2,1-benzisoxazoles in a 34-97% isolated yield.
Efficient total syntheses of phytoalexin and (±)-paniculidine B and C based on the novel methodology for the preparation of 1-methoxyindoles
Selvakumar,Rajulu, G. Govinda
, p. 4429 - 4432 (2007/10/03)
A general route to 2-unsubstituted-1-methoxyindoles, based on our methodology for the synthesis of 1-methoxyindoles, is reported. This synthesis renders accessibility to a variety of natural products possessing the said skeleton. A direct synthesis of phy
Syntheses of Functionalised Pyridoindoles
Forbes, Ian T.,Johnson, Christopher N.,Thompson, Mervyn
, p. 275 - 282 (2007/10/02)
Two complementary routes for the synthesis of highly functionalised pyridoindoles are described, starting from the readily available 2-amino-3-cyano-1-(4-methoxybenzyl)tetrahydroindole and methyl 2-aminoindole-3-carboxylate, respectively.The use of
Xn:Harmful;
