30611-26-8 Usage
Description
1-(4-HYDROXYMETHYL-PHENYL)-PENTAN-1-ONE, with the molecular formula C12H16O2, is a ketone derivative characterized by a phenyl group and a hydroxymethyl group attached to a pentan-1-one backbone. This chemical compound is known for its potential applications in the synthesis of complex organic molecules and in medicinal chemistry. It is crucial to handle and utilize this compound with caution, adhering to safety guidelines and regulations to minimize any possible risks.
Uses
Used in Organic Synthesis:
1-(4-HYDROXYMETHYL-PHENYL)-PENTAN-1-ONE is used as a building block for the synthesis of complex organic molecules, leveraging its unique structure and functional groups to create a variety of compounds with diverse properties and applications.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 1-(4-HYDROXYMETHYL-PHENYL)-PENTAN-1-ONE serves as a valuable intermediate or precursor in the development of new pharmaceuticals. Its structural features can be exploited to design and synthesize bioactive molecules with potential therapeutic benefits.
Used in Pharmaceutical Industry:
1-(4-HYDROXYMETHYL-PHENYL)-PENTAN-1-ONE is used as a key component in the formulation of pharmaceutical products, contributing to the development of novel drugs with improved efficacy and safety profiles.
Used in Chemical Research:
1-(4-HYDROXYMETHYL-PHENYL)-PENTAN-1-ONE is also utilized in chemical research as a model system for studying various reaction mechanisms, exploring new synthetic routes, and understanding the relationship between molecular structure and chemical reactivity.
Check Digit Verification of cas no
The CAS Registry Mumber 30611-26-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,6,1 and 1 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 30611-26:
(7*3)+(6*0)+(5*6)+(4*1)+(3*1)+(2*2)+(1*6)=68
68 % 10 = 8
So 30611-26-8 is a valid CAS Registry Number.
InChI:InChI=1/C12H16O2/c1-2-3-4-12(14)11-7-5-10(9-13)6-8-11/h5-8,13H,2-4,9H2,1H3
30611-26-8Relevant articles and documents
Chemoselective reduction of aldehydes: Via a combination of NaBH4 and acetylacetone
Sui, Guoqing,Lv, Qingyun,Song, Xiaoqing,Guo, Huihui,Dai, Jiatong,Ren, Li,Lee, Chi-Sing,Zhou, Wenming,Hao, Hong-Dong
, p. 15793 - 15796 (2019/10/19)
A bench-stable combination of NaBH4-acetylacetone was developed for the efficient chemoselective reduction of aldehydes in the presence of ketones. This method offers a useful synthetic protocol for distinguishing carbonyl reaction sites, and its synthetic utility is reflected by its moisture tolerance and high efficiency in a variety of complex settings.
