6468-19-5 Usage
Uses
Used in Pharmaceutical Synthesis:
2,4-dimethoxy-5-nitro-benzaldehyde is utilized as an intermediate in the synthesis of various pharmaceuticals. Its unique structure allows for the development of new drug candidates, contributing to the advancement of medicinal chemistry.
Used in Organic Chemistry:
2,4-dimethoxy-5-nitro-benzaldehyde also serves as a reagent in organic chemistry reactions, facilitating the synthesis of a wide range of organic compounds. Its presence in these reactions can lead to the formation of new molecules with potential applications in various fields.
Used in Organic Synthesis:
2,4-dimethoxy-5-nitro-benzaldehyde is employed as a building block in organic synthesis, enabling the construction of more complex molecules. Its versatility in this context is a testament to its unique chemical properties, which make it a valuable asset in the field of organic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 6468-19-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,4,6 and 8 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6468-19:
(6*6)+(5*4)+(4*6)+(3*8)+(2*1)+(1*9)=115
115 % 10 = 5
So 6468-19-5 is a valid CAS Registry Number.
InChI:InChI=1/C9H9NO5/c1-14-8-4-9(15-2)7(10(12)13)3-6(8)5-11/h3-5H,1-2H3
6468-19-5Relevant academic research and scientific papers
Convergent synthesis of Carpatamide-A: Cytotoxic arylamine derivative from marine derived Streptomyces sp.
Burman, Rohani Prasad,Gupta, Shantanu,Bhatti, Jyoti,Verma, Krishan,Rajak, Devendra,Gill, Manjinder Singh
, p. 1 - 11 (2018/05/25)
First total synthesis of carpatamide-A 7a, cytotoxic arylamine derivative isolated from marine derived Streptomyces sp., was achieved in twelve steps with overall yield of 24% with seven longest linear steps. In the penultimate step, dienoic acid 13 and a
Cerium(IV)-induced nitration of cinnamic acids. Novel remote electrophilic substitution
Peterson, John R.,Do, Hoang D.,Dunham, Andrew J.
, p. 1670 - 1674 (2007/10/02)
The treatment of (E)-3,4-dimethoxycinnamic acid with ceric amonium nitrate in trifluoroacetic acid afforded (E)1,2-dimethoxy-4-nitro-5-(2-nitroethenyl)benzene in 79percent yield.The unusual ipso substitution of the carboxylic acid moiety by a nitro functional center illustrated a new reaction manifold of cerium(IV).Six cinnamic acids were examined to ascertain the generality of the transformation.The bidentate nitrato structure of the metal salt is believed to account for the nitrating ability of this system.
