6077-72-1 Usage
Uses
Used in Pharmaceutical Industry:
2-METHYLCYCLOPROPANEMETHANOL is used as a chemical intermediate for the synthesis of various pharmaceutical compounds. Its unique structure allows for the development of new drugs with specific therapeutic properties.
Used in Chemical Research:
2-METHYLCYCLOPROPANEMETHANOL is used as a research compound in the investigation of microsomal cytochrome P-450 hydroxylation of hydrocarbons. This application helps in understanding the metabolic pathways of various hydrocarbons and their potential effects on human health.
Used in Material Science:
2-METHYLCYCLOPROPANEMETHANOL can be used as a building block for the development of new materials with specific properties, such as improved strength, flexibility, or chemical resistance. Its unique structure and chemical properties make it a valuable component in the design and synthesis of advanced materials.
Used in Environmental Science:
2-METHYLCYCLOPROPANEMETHANOL can be employed in the study of environmental pollutants and their degradation pathways. Understanding the interaction of 2-METHYLCYCLOPROPANEMETHANOL with environmental factors can provide insights into the fate and transport of similar pollutants in the environment.
Used in Analytical Chemistry:
2-METHYLCYCLOPROPANEMETHANOL can be used as a reference compound in various analytical techniques, such as gas chromatography, mass spectrometry, and nuclear magnetic resonance (NMR) spectroscopy. Its clear and colorless nature makes it an ideal candidate for calibration and method development in these analytical methods.
Check Digit Verification of cas no
The CAS Registry Mumber 6077-72-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,7 and 7 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6077-72:
(6*6)+(5*0)+(4*7)+(3*7)+(2*7)+(1*2)=101
101 % 10 = 1
So 6077-72-1 is a valid CAS Registry Number.
InChI:InChI=1/C5H10O/c1-4-2-5(4)3-6/h4-6H,2-3H2,1H3/t4-,5-/m0/s1
6077-72-1Relevant academic research and scientific papers
The Thermal Decomposition of Diazirines: 3-(3-Methyldiazirin-3-yl)propan-1-ol and 3-(3-Methyldiazirin-3-yl)propanoic Acid
Stevens, Ian D. R.,Liu, Michael T. H.,Soundararajan, N.,Paike, N.
, p. 661 - 667 (2007/10/02)
The thermolyses of 3-(3-methyldiazirin-3-yl)propan-1-ol (1) and 3-(3-methyldiazirin-3-yl)propanoic acid (2) have been studied in solution over the temperature range 96-125 deg C.The reactions are unimolecular and fit linear Arrhenius plots with k(1)=1013.85+/-0.69exp-1/RT>s-1 and k(2)=1012.38+/-0.43exp-1/RT>s-1.The major products are the alkenes derived from the corresponding carbenes MeC2.CH2CH2CH2OH (3) and MeC2.CH2CH2CO2H (4).The new rate data, taken together with previous work, tend to confirm that diazirine thermolysis involves ring opening to a "complex" followed either by nitrogen loss or by isomerization to a diazo compound.Whereas (1) gives no product of closure onto oxygen, the acid (2) affords about 5percent γ-valerolactone.
THE BARRIER FOR 1,2 HYDROGEN SHIFT IN DIALKYL CARBENES
Stevens, Ian D. R.,Liu, Michael T. H.,Soundararajan, N.,Paike, N.
, p. 481 - 484 (2007/10/02)
The products from the thermolysis of 4-diazirinopentanoic acid (2) allow the estimate of an experimental value for the Ea = 1.1 +/- 1 kcal.mol-1 for the barrier height for 1,2 H shift in dialkyl carbenes.
