3607-48-5 Usage
Description
(Iodoimino)methanone, with the molecular formula CH2INO, is a chemical compound known for its reactivity and instability. This yellow-colored compound is widely utilized in organic synthesis, particularly for its ability to add iodine to carbon-carbon double bonds. Due to its potential to decompose and release toxic iodine fumes, it is handled with caution and typically stored and managed under inert gas conditions.
Uses
Used in Organic Synthesis:
(Iodoimino)methanone is used as a reagent for the addition of iodine to carbon-carbon double bonds, which is crucial in the formation of various organic compounds. Its ability to facilitate this reaction makes it a valuable tool in the synthesis of a range of chemical products.
Used in Pharmaceutical Applications:
(Iodoimino)methanone is employed as a key intermediate in the preparation of iodinated heterocycles, which are significant in the pharmaceutical industry. These heterocycles have potential applications in the development of new drugs and therapeutic agents.
Used in Materials Science:
(iodoimino)methanone has also been studied for its potential applications in materials science. Its unique properties and reactivity make it a candidate for the development of new materials with specific characteristics and potential uses in various industries.
Used in Chemical Research:
(Iodoimino)methanone serves as a subject of interest in chemical research, where its properties and reactions are explored to further understand its potential applications and to develop methods for safer handling and utilization in various chemical processes.
Check Digit Verification of cas no
The CAS Registry Mumber 3607-48-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,6,0 and 7 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 3607-48:
(6*3)+(5*6)+(4*0)+(3*7)+(2*4)+(1*8)=85
85 % 10 = 5
So 3607-48-5 is a valid CAS Registry Number.
3607-48-5Relevant articles and documents
Photochemistry of BrNCO and INCO
Liu, X.,Gilbert, J. V.,Coombe, R. D.
, p. 171 - 176 (1989)
The absorption spectra of BrNCO and INCO in the region 160-400 nm are continuous in nature,and photolysis of these molecules with pulsed excimer lasers leads to dissociation.Photolysis of BrNCO and INCO at 308 and 351 nm, respectively, produces vibrationally cold ground state NCO radicals.Weak NCO A 2Σ+ X 2Π emission results from two-photon absorption processes at these wavelengths.Photolysis of BrNCO and INCO at 193 and 222 nm, respectively, produces intense NCO A 2Σ+ X 2Π emission.The NCO(A) is a direct one-photon photofragment in each case, and has considerable vibrational excitation.The yield of NCO(A) from BrNCO photolysis at 193 nm is approximately 16percent; the yield of NCO(A) from INCO photolysis at 222 nm is near 13percent.From the production of NCO(a) at these wavelengths and the short wavelength limit of the NCO A 2Σ+ X 2Π emission, limits on the heats of formation of these molecules are found to be ΔHf(BrNCO) -1.7 kcal mol-1 and ΔHf(INCO) 10.9 kcal mol-1.These results demonstrate the preference of the halogen isocyanates for dissociation to double fragments by scission of the nitrogen-halogen bond, in contrast to the analogous halogen azides which photodissociate to singlet or triplet fragments.
THE INFRARED SPECTRA OF THE HALOGEN ISOCYANATE AND THIOCYANATE VAPOR MOLECULES
Devore, T. C.
, p. 287 - 304 (2007/10/02)
Fourier transform infrared spectroscopy has been used to investigate the IR spectra of the XNCO (X = Cl, Br, I, CN), the XSCN (X = Cl, Br, I) and the NCNCS vapor molecules from 4800 to 400 cm-1.Vibrational frequencies have been determined for e
