2385-38-8 Usage
Description
1-Benzyl-2-imidazolidinone (SALTDATA: FREE), also known as 1-(Phenylmethyl)-2-imidazolidinone, is an organic compound with the CAS number 2385-38-8. It is an off-white solid and is primarily used in the field of organic synthesis due to its unique chemical properties.
Uses
Used in Organic Synthesis:
1-Benzyl-2-imidazolidinone (SALTDATA: FREE) is used as a synthetic building block for the creation of various organic compounds. Its unique structure allows it to be a versatile component in the synthesis of a wide range of molecules, including pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 1-benzyl-2-imidazolidinone (SALTDATA: FREE) is used as an intermediate in the synthesis of various drugs. Its presence in the molecular structure can contribute to the desired pharmacological properties of the final product, making it a valuable asset in drug development.
Used in Agrochemical Industry:
1-Benzyl-2-imidazolidinone (SALTDATA: FREE) is also utilized in the agrochemical industry for the synthesis of pesticides, herbicides, and other crop protection agents. Its incorporation into these compounds can enhance their effectiveness and selectivity, leading to improved agricultural productivity and crop protection.
Used in Specialty Chemicals:
In the specialty chemicals sector, 1-benzyl-2-imidazolidinone (SALTDATA: FREE) is employed in the development of various high-value products, such as dyes, fragrances, and additives. Its unique chemical properties make it an essential component in the synthesis of these specialty chemicals, contributing to their performance and functionality.
Check Digit Verification of cas no
The CAS Registry Mumber 2385-38-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,8 and 5 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2385-38:
(6*2)+(5*3)+(4*8)+(3*5)+(2*3)+(1*8)=88
88 % 10 = 8
So 2385-38-8 is a valid CAS Registry Number.
InChI:InChI=1/C10H12N2O/c13-10-11-6-7-12(10)8-9-4-2-1-3-5-9/h1-5H,6-8H2,(H,11,13)
2385-38-8Relevant articles and documents
1-ACRYLOYLIMIDAZOLIDINE-2-ONE COMPOUND
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Paragraph 0065-0067, (2021/03/03)
To provide a compound that is expected to be applied to cell culture materials, temperature-responsive polymer materials and the like.SOLUTION: The present invention relates to a 1-acryloylimidazolidine-2-one compound represented by formula (1) (where R1a is a hydrogen atom, a C1 to 4 alkyl group, a benzyl group or an oxyalkyl group represented by formula (2). R2a is a hydrogen atom or a C1 to 4 alkyl group. R3a is a hydrogen atom or a methyl group).SELECTED DRAWING: None
Silver-Catalyzed, N-Formylation of Amines Using Glycol Ethers
King, Bradley H.,Wang, Michelle L.,Jesse, Kate A.,Kaur, Guneet,Tran, Brianna,Walser-Kuntz, Ryan,Iafe, Robert G.,Wenzel, Anna G.
, p. 13256 - 13263 (2020/11/26)
A silver-catalyzed protocol was found to afford the N-formylation of amines in moderate-to-good yields. Ethylene glycol-derived, oligomeric ethers were found to function as the formylating agent, with 1,4-dioxane affording the best results. This reaction does not require the use of stoichiometric activating reagents, and avoids the use of explosive reagents or toxic gases, such as CO, as the C1 synthon. Mechanistic studies indicate a single-electron transfer-based pathway. This work highlights the ability of silver to participate in unexpected reaction pathways.
3-(Triflyloxy)benzynes Enable the Regiocontrolled Cycloaddition of Cyclic Ureas to Synthesize 1,4-Benzodiazepine Derivatives
Kaneko, Hideki,Ikawa, Takashi,Yamamoto, Yuta,Arulmozhiraja, Sundaram,Tokiwa, Hiroaki,Akai, Shuji
supporting information, p. 943 - 948 (2018/02/26)
A versatile synthesis of 1,4-benzodiazepine derivatives through the reaction of various 3-(trifluoromethanesulfonyloxy)benzynes with N -(p -toluenesulfonyl)imidazolidin-2-ones is reported. This reaction system provides a 1,4-benzodiazepine bearing a trifluoromethanesulfonyloxy group as a single regioisomer among the four possible regioisomers.
