2612-29-5 Usage
Description
2-Ethylpropane-1,3-diol is an organic compound with the chemical formula C5H12O2. It is a colorless liquid with a slight odor and is soluble in water. It is also known as 2-ethyl-1,3-propanediol or 2-ethylpropane-1,3-diyl diethanol.
Uses
Used in Pharmaceutical Industry:
2-Ethylpropane-1,3-diol is used as an intermediate in the synthesis of Peloruside A related compounds, which are novel antimitotic agents with Paclitaxel (P132500)-like microtubule-stabilizing activity. These compounds have potential applications in the development of new cancer therapies.
Used in Chemical Synthesis:
2-Ethylpropane-1,3-diol can be used as a building block in the synthesis of various organic compounds, including pharmaceuticals, agrochemicals, and specialty chemicals. Its unique structure allows for the formation of diverse products through chemical reactions.
Used in Solvent Applications:
Due to its solubility in water and other solvents, 2-ethylpropane-1,3-diol can be used as a solvent in various industrial processes, such as in the production of coatings, adhesives, and sealants.
Used in Fuel Additives:
2-Ethylpropane-1,3-diol can be used as a fuel additive to improve the performance and efficiency of fuels in internal combustion engines. It can also be used as a component in the production of biofuels.
Used in Personal Care Products:
2-Ethylpropane-1,3-diol can be used as a humectant in personal care products, such as cosmetics, lotions, and creams, to help retain moisture and improve the texture of the products.
Check Digit Verification of cas no
The CAS Registry Mumber 2612-29-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,6,1 and 2 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2612-29:
(6*2)+(5*6)+(4*1)+(3*2)+(2*2)+(1*9)=65
65 % 10 = 5
So 2612-29-5 is a valid CAS Registry Number.
InChI:InChI=1/C5H12O2/c1-2-5(3-6)4-7/h5-7H,2-4H2,1H3
2612-29-5Relevant articles and documents
INDOLE DERIVATIVES AS ALPHA-1 -ANTITRYPSIN MODULATORS FOR TREATING ALPHA-1 -ANTITRYPSIN DEFICIENCY (AATD)
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Paragraph 00234; 00316; 00793, (2021/10/11)
Indole derivatives as alpha-l-antitrypsin modulators for treating alpha-l-antitrypsin deficiency (AATD).
SULPHONAMIDES AND COMPOSITIONS THEREOF FOR TREATING CONDITIONS ASSOCIATED WITH NLRP ACTIVITY
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Page/Page column 537, (2019/05/10)
In one aspect, compounds of Formula AA, or a pharmaceutically acceptable salt thereof, are featured: wherein the variables shown in Formula AA can be as defined anywhere herein. Compounds AA are modulators of NLRP1 and/or NLRP3
Synthesis of Enantiomerically Enriched 2-Hydroxymethylalkanoic Acids by Oxidative Desymmetrisation of Achiral 1,3-Diols Mediated by Acetobacter aceti
Brenna, Elisabetta,Cannavale, Flavia,Crotti, Michele,De Vitis, Valerio,Gatti, Francesco G.,Migliazza, Gaia,Molinari, Francesco,Parmeggiani, Fabio,Romano, Diego,Santangelo, Sara
, p. 3796 - 3803 (2016/12/24)
The stereoselective desymmetrisation of achiral 2-alkyl-1,3-diols is performed by oxidation of one of the two enantiotopic primary alcohol moieties by means of Acetobacter aceti MIM 2000/28 to afford the corresponding chiral 2-hydroxymethyl alkanoic acids (up to 94 % ee). The procedure, carried out in aqueous medium under mild conditions of pH, temperature and pressure, contributes to enlarge the portfolio of enzymatic oxidations available to organic chemists for the development of sustainable manufacturing processes.