49675-78-7 Usage
Uses
Used in Pharmaceutical Industry:
(3Z)-5-BROMO-1H-INDOLE-2,3-DIONE 3-OXIME is used as an intermediate in the synthesis of various pharmaceuticals. Its distinctive structural features and potential biological activities make it a valuable component in the development of new drugs.
Used in Agrochemical Industry:
(3Z)-5-BROMO-1H-INDOLE-2,3-DIONE 3-OXIME is also used in the preparation of agrochemicals. Its reactivity and unique properties contribute to the creation of effective compounds for agricultural applications.
Used in Organic Synthesis:
(3Z)-5-BROMO-1H-INDOLE-2,3-DIONE 3-OXIME serves as an important building block in organic synthesis. Its versatility and reactivity, particularly due to the bromine substituent, make it suitable for the synthesis of complex organic molecules.
Check Digit Verification of cas no
The CAS Registry Mumber 49675-78-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,9,6,7 and 5 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 49675-78:
(7*4)+(6*9)+(5*6)+(4*7)+(3*5)+(2*7)+(1*8)=177
177 % 10 = 7
So 49675-78-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H5BrN2O2/c9-4-1-2-6-5(3-4)7(11-13)8(12)10-6/h1-3,13H,(H,10,11,12)
49675-78-7Relevant academic research and scientific papers
Acylating and arylsulfonylating ability of O-derivatives of isatin 3-oximes
Stankevicius,Terentiev,Janushene,Savickas
, p. 98 - 104 (2007/10/03)
O-Acyl and O-arylsulfonyl derivatives of isatin 3-oximes have been synthesized and their interaction with alcohols and amines has been investigated. It was established that none of the esters of 1-substituted isatin 3-oximes reacted with the indicated nucleophiles. 1-Unsubstituted O-aryl and O-arylsulfonyl derivatives react with amines as acylating agents even at room temperature, but O-acetyl derivatives only on heating. Acylamides or arylsulfamides respectively are formed in this way. O-Acyl derivatives do not react with alcohols at room temperature. Only O-benzoyl derivatives form ethyl benzoate on heating in ethanol. A comparative analysis of mass spectrometric data on the processes of acylation and arylsulfonylation is given.
