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25574-04-3

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25574-04-3 Usage

Description

1-(4-METHYLPHENYL)-1-PROPANOL 97, also known as 1-(4-Methylphenyl)propan-1-ol, is a secondary alcohol derivative that can be synthesized by the reduction of 4′-methylpropiophenone. It is characterized by its unique chemical structure, which features a methyl group attached to a phenyl ring and a propyl chain connected to a hydroxyl group. 1-(4-METHYLPHENYL)-1-PROPANOL 97 has potential applications in various industries due to its distinct properties.

Uses

1. Used in the Chemical Synthesis Industry:
1-(4-METHYLPHENYL)-1-PROPANOL 97 is used as a key intermediate in the synthesis of alkyne compounds through a catalytic asymmetric cross-coupling reaction. This application is significant because it allows for the creation of new and complex molecules with potential uses in various fields, such as pharmaceuticals, materials science, and agrochemicals.
2. Used in the Pharmaceutical Industry:
1-(4-METHYLPHENYL)-1-PROPANOL 97 can be utilized as a building block for the development of new drugs. Its unique structure and reactivity make it a valuable component in the design and synthesis of novel pharmaceutical compounds, potentially leading to the discovery of new treatments for various diseases and conditions.
3. Used in the Chiral Compounds Industry:
The racemic form of 1-(4-METHYLPHENYL)-1-PROPANOL 97 can be resolved through oxidative kinetic resolution in the presence of chiral polymeric Mn(III) salen complexes. This process is essential in obtaining enantiomerically pure compounds, which are crucial for the development of chiral drugs with improved efficacy and reduced side effects.

Check Digit Verification of cas no

The CAS Registry Mumber 25574-04-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,5,7 and 4 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 25574-04:
(7*2)+(6*5)+(5*5)+(4*7)+(3*4)+(2*0)+(1*4)=113
113 % 10 = 3
So 25574-04-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H14O/c1-3-10(11)9-6-4-8(2)5-7-9/h4-7,10-11H,3H2,1-2H3

25574-04-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-methylphenyl)propan-1-ol

1.2 Other means of identification

Product number -
Other names 1-(p-Tolyl)-1-propanol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:25574-04-3 SDS

25574-04-3Relevant articles and documents

Copper-Catalyzed Enantioconvergent Cross-Coupling of Racemic Alkyl Bromides with Azole C(sp2)?H Bonds

Chang, Xiao-Yong,Chen, Ji-Jun,Gu, Qiang-Shuai,Jiang, Sheng-Peng,Li, Zhong-Liang,Liu, Lin,Liu, Xiao-Dong,Liu, Xin-Yuan,Su, Xiao-Long,Wang, Fu-Li,Yang, Chang-Jiang,Ye, Liu

supporting information, p. 380 - 384 (2020/10/30)

The development of enantioconvergent cross-coupling of racemic alkyl halides directly with heteroarene C(sp2)?H bonds has been impeded by the use of a base at elevated temperature that leads to racemization. We herein report a copper(I)/cinchona-alkaloid-derived N,N,P-ligand catalytic system that enables oxidative addition with racemic alkyl bromides under mild conditions. Thus, coupling with azole C(sp2)?H bonds has been achieved in high enantioselectivity, affording a number of potentially useful α-chiral alkylated azoles, such as 1,3,4-oxadiazoles, oxazoles, and benzo[d]oxazoles as well as 1,3,4-triazoles, for drug discovery. Mechanistic experiments indicated facile deprotonation of an azole C(sp2)?H bond and the involvement of alkyl radical species under the reaction conditions.

2,2′-Bipyridine-α,α′-trifluoromethyl-diol ligand: Synthesis and application in the asymmetric Et2Zn alkylation of aldehydes

Lauzon, Samuel,Ollevier, Thierry

supporting information, p. 11025 - 11028 (2021/11/03)

A chiral 2,2′-bipyridine ligand (1) bearing α,α′-trifluoromethyl-alcohols at 6,6′-positions was designed in five steps affording either the R,R or S,S enantiomer with excellent stereoselectivities, i.e. 97% de, >99% ee and >99.5% de, >99.5% ee, respectively. The key step for reaching high levels of stereoselectivity was demonstrated to be the resolution of the α-CF3-alcohol using (S)-ibuprofen as the resolving agent. An initial application for the 2,2′-bipyridine-α,α′-CF3-diol ligand was highlighted in the ZnII-catalyzed asymmetric ethylation reaction of aromatic, heteroaromatic, and aliphatic aldehydes. Synergistic electron deficiency and steric hindrance properties of the newly developed ligand afforded the corresponding alcohols in good to excellent yields (up to 99%) and enantioselectivities (up to 95% ee). As observed from single crystal diffraction analysis, the complexation of the 2,2′-bipyridine-α,α′-CF3-diol ligand generates an unusual hexacoordinated ZnII.

Rhodium coordination compound as well as preparation method and application thereof

-

Paragraph 0133-0135, (2020/09/09)

The invention discloses a rhodium coordination compound as well as a preparation method and application thereof. The structure of the rhodium coordination compound is shown as a formula I which is described in the specification, wherein R is one of H and C1-C6 alkyl, and X is halogen. The rhodium coordination compound can efficiently catalyze a carbonyl transfer hydrogenation reaction to obtain corresponding alcohol, and meanwhile, the preparation method has the advantages of simple process and simplicity and convenience in operation.

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