106-67-2 Usage
Description
1-Pentanol,2-ethyl-4-methylis an organic compound with the molecular formula C7H16O. It is a colorless liquid with a distinctive odor and is classified as a secondary alcohol. 1-Pentanol,2-ethyl-4-methylis characterized by its five-carbon chain with a hydroxyl group (-OH) at the first carbon, an ethyl group (-CH2CH3) at the second carbon, and a methyl group (-CH3) at the fourth carbon.
Uses
1. Used in Diagnostic Applications:
1-Pentanol,2-ethyl-4-methylis used as a diagnostic chemical for identifying ratoon stunting disease in sugar cane. The compound's volatility allows it to be easily detected and analyzed, making it a valuable tool in the early detection and monitoring of this disease, which can significantly impact sugar cane productivity and quality.
2. Used in Chemical Synthesis:
1-Pentanol,2-ethyl-4-methylcan be utilized as an intermediate in the synthesis of various organic compounds, such as fragrances, pharmaceuticals, and agrochemicals. Its unique structural features make it a versatile building block for creating a wide range of products.
3. Used in Flavor and Fragrance Industry:
1-Pentanol,2-ethyl-4-methylis used as a component in the creation of artificial flavors and fragrances due to its distinct odor. It can be found in the formulation of various consumer products, such as perfumes, cosmetics, and food additives, where it contributes to the overall sensory experience.
4. Used in Solvent Applications:
As a polar organic compound, 1-Pentanol,2-ethyl-4-methylcan act as a solvent for a variety of substances, including other organic compounds, in various industrial processes. Its solubility properties make it suitable for use in the pharmaceutical, chemical, and materials science industries.
5. Used in Fuel Additives:
1-Pentanol,2-ethyl-4-methylcan be employed as an additive in the fuel industry to improve the performance and efficiency of fuels. Its ability to mix with hydrocarbons and other fuel components can enhance the combustion process, leading to better engine performance and reduced emissions.
Check Digit Verification of cas no
The CAS Registry Mumber 106-67-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,0 and 6 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 106-67:
(5*1)+(4*0)+(3*6)+(2*6)+(1*7)=42
42 % 10 = 2
So 106-67-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H18O/c1-4-8(6-9)5-7(2)3/h7-9H,4-6H2,1-3H3
106-67-2Relevant articles and documents
Hudson et al.
, p. 63,65 (1956)
Syntheses and evaluation of anticonvulsant activity of novel branched alkyl carbamates
Hen, Naama,Bialer, Meir,Yagen, Boris
experimental part, p. 2835 - 2845 (2012/06/15)
A novel class of 19 carbamates was synthesized, and their anticonvulsant activity was comparatively evaluated in the rat maximal electroshock (MES) and subcutaneous metrazol (scMet) seizure tests and pilocarpine-induced status epilepticus (SE) model. In spite of the alkyl-carbamates' close structural features, only compounds 34, 38, and 40 were active at the MES test. The analogues 2-ethyl-3-methyl-butyl-carbamate (34) and 2-ethyl-3-methyl-pentyl- carbamate (38) also exhibited potent activity in the pilocarpine-SE model 30 min postseizure onset. Extending the aliphatic side chains of homologous carbamates from 7 to 8 (34 to 35) and from 8 to 9 carbons in the homologues 38 and 43 decreased the activity in the pilocarpine-SE model from ED50 = 81 mg/kg (34) to 94 mg/kg (35) and from 96 mg/kg (38) to 114 mg/kg (43), respectively. The most potent carbamate, phenyl-ethyl-carbamate (47) (MES ED50 = 16 mg/kg) contains an aromatic moiety in its structure. Compounds 34, 38, 40, and 47 offer the optimal efficacy-safety profile and, consequently, are promising candidates for development as new antiepileptics.
