73428-04-3 Usage
Uses
Used in Chemical Synthesis:
3-Nitronaphthalene-2-methanol is used as a key intermediate in the synthesis of various organic compounds, particularly those involving naphthalene derivatives. Its presence in the molecule allows for further functionalization and modification, making it a versatile building block for the development of new chemicals and materials.
Used in Pharmaceutical Industry:
3-Nitronaphthalene-2-methanol is used as a starting material for the development of pharmaceutical compounds. Its unique structure and reactivity make it a promising candidate for the design and synthesis of novel drugs with potential therapeutic applications.
Used in Photochemistry:
As a photocleavable protecting group for carboxylic acids, 3-Nitronaphthalene-2-methanol plays a crucial role in photochemistry. It can be used to protect carboxylic acid functional groups during chemical reactions, allowing for selective deprotection under specific light conditions. This property is particularly useful in the synthesis of complex organic molecules and in the development of controlled drug release systems.
Used in Dye Synthesis:
The yellow crystalline nature of 3-Nitronaphthalene-2-methanol makes it a potential candidate for the development of new dyes and pigments. Its unique color properties can be exploited to create novel dyes with specific applications in various industries, such as textiles, plastics, and printing.
Check Digit Verification of cas no
The CAS Registry Mumber 73428-04-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,4,2 and 8 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 73428-04:
(7*7)+(6*3)+(5*4)+(4*2)+(3*8)+(2*0)+(1*4)=123
123 % 10 = 3
So 73428-04-3 is a valid CAS Registry Number.
InChI:InChI=1/C11H9NO3/c13-7-10-5-8-3-1-2-4-9(8)6-11(10)12(14)15/h1-6,13H,7H2
73428-04-3Relevant articles and documents
NUCLEIC ACID BINDING COMPOUNDS, METHODS OF MAKING, AND USE THEREOF
-
Page/Page column 46-47, (2012/07/14)
The present invention relates to oligomer compounds, including dimers and trimers, formed by a disulfide, sulfinyl thio, olefin or hydrocarbon bond, or a hydrazone exchange bond between two or more monomers. Methods of making the monomers and the oligomers is also disclosed. Use of the compounds for inhibiting the activity of target RNA molecules, particularly those having a secondary structure that include a stem or stem-loop formation. Dimer compounds capable of inhibiting the activity of an HIV-1 RNA frameshifting stem-loop and a (CUG)n expanded repeat stem- loop are disclosed, as are methods of treating diseases associated with these target RNA molecules.
Arylmethyl radicals from arylmethoxybromodiazirines
Moss, Robert A.,Fu, Xiaolin
, p. 3353 - 3356 (2007/10/03)
(Chemical Equation Presented) Photolytic decompositions of 3-arylmethoxy-3-bromodiazirines afford arylmethyl radicals by homolyses of the diazirines' excited states.
The Reaction of Phthalaldehydes with 3-Nitropropionates. A Simple Route to 3-Nitro-2-naphthoic Acids
Kienzle, Frank
, p. 2364 - 2369 (2007/10/02)
3-Nitro-propionates condense with phthalaldehydes and related compounds in the presence of a base to give 3-nitro-2-naphthoic acids.
Plant antitumor agents: Synthesis and biological activity of camptothecin analogues
Wani,Ronman,Lindley,Wall
, p. 554 - 560 (2007/10/02)
Four analogues, 10-methoxy (20), 12-aza (29), benz[j] (36), and 18-methoxy (38), of camptothecin were obtained by total synthesis. The two water-soluble analogues, 10-[(carboxymethyl)oxy] (24) and 10-[2'-(diethylamino)-ethoxy]-20(S)-camptothecin (26), wit
