612825-76-0 Usage
Description
(4-Iodo-3-nitro-phenyl)-Methanol is a chemical compound with the molecular formula C7H6INO3. It is a derivative of phenyl alcohol that contains an iodo and a nitro group attached to the phenyl ring. (4-Iodo-3-nitro-phenyl)-Methanol is known for its unique chemical structure, which makes it a valuable tool in various fields of chemistry and biochemistry.
Uses
Used in Organic Synthesis:
(4-Iodo-3-nitro-phenyl)-Methanol is used as a reagent in organic synthesis for the production of various pharmaceuticals, agrochemicals, and fine chemicals. Its unique structure allows it to be a versatile building block in the synthesis of complex organic molecules.
Used in Medicinal and Biochemical Research:
Due to its potential biological activities, (4-Iodo-3-nitro-phenyl)-Methanol is used as a valuable tool in medicinal and biochemical research. Its unique chemical properties make it suitable for studying various biological processes and developing new therapeutic agents.
Used in Chemical Industry:
(4-Iodo-3-nitro-phenyl)-Methanol is used in the chemical industry for various applications, including the synthesis of dyes, pigments, and other specialty chemicals. Its unique structure and reactivity make it a useful intermediate in the production of these materials.
Check Digit Verification of cas no
The CAS Registry Mumber 612825-76-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,1,2,8,2 and 5 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 612825-76:
(8*6)+(7*1)+(6*2)+(5*8)+(4*2)+(3*5)+(2*7)+(1*6)=150
150 % 10 = 0
So 612825-76-0 is a valid CAS Registry Number.
612825-76-0Relevant articles and documents
Oxidative Approach Enables Efficient Access to Cyclic Azobenzenes
Maier, Martin S.,Hüll, Katharina,Reynders, Martin,Matsuura, Bryan S.,Leippe, Philipp,Ko, Tongil,Sch?ffer, Lukas,Trauner, Dirk
supporting information, p. 17295 - 17304 (2019/11/03)
Azobenzenes are versatile photoswitches that have found widespread use in a variety of fields, ranging from photopharmacology to the material sciences. In addition to regular azobenzenes, the cyclic diazocines have recently emerged. Although diazocines have fascinating conformational and photophysical properties, their use has been limited by their synthetic accessibility. Herein, we present a general, high-yielding protocol that relies on the oxidative cyclization of dianilines. In combination with a modular substrate synthesis, it allows for rapid access to diversely functionalized diazocines on gram scales. Our work systematically explores substituent effects on the photoisomerization and thermal relaxation of diazocines. It will enable their incorporation into a wide variety of functional molecules, unlocking the full potential of these emerging photoswitches. The method can be applied to the synthesis of a new cyclic azobenzene with a nine-membered central ring and distinct properties.
Catalytic asymmetric synthesis of the central tryptophan residue of celogentin C
Castle, Steven L.,Srikanth
, p. 3611 - 3614 (2007/10/03)
(Equation presented) Chiral phase-transfer catalyst 5 containing an electron-deficient trifluorobenzyl moiety promoted the alkylation of glycine derivative 6 with propargyl bromide 7a in good yield and excellent ee. The resulting propargyl glycine 8 was c
