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114837-50-2

114837-50-2

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114837-50-2 Usage

Description

1-(2-bromophenyl)prop-2-en-1-ol is a chemical compound with the molecular formula C9H9BrO. It is an organic compound that contains a bromine atom, a phenyl group, and a hydroxyl group attached to a propene chain. 1-(2-broMophenyl)prop-2-en-1-ol is known for its unique chemical structure and properties, which contribute to its potential applications in various fields.

Uses

Used in Organic Synthesis:
1-(2-bromophenyl)prop-2-en-1-ol is used as a building block in organic synthesis for the creation of more complex molecules. Its unique structure allows for a wide range of reactions, making it a versatile compound in the field of organic chemistry.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 1-(2-bromophenyl)prop-2-en-1-ol is used as a key intermediate in the development of new drugs. Its chemical properties make it a promising candidate for the synthesis of various pharmaceutical compounds.
Used in Materials Science:
1-(2-bromophenyl)prop-2-en-1-ol may have potential applications in the field of materials science, where its unique structure could be utilized to create novel materials with specific properties.
Used as a Chemical Intermediate:
In the manufacturing of various products, 1-(2-bromophenyl)prop-2-en-1-ol serves as a chemical intermediate. Its role in the production process is crucial for the synthesis of a range of specialty chemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 114837-50-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,8,3 and 7 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 114837-50:
(8*1)+(7*1)+(6*4)+(5*8)+(4*3)+(3*7)+(2*5)+(1*0)=122
122 % 10 = 2
So 114837-50-2 is a valid CAS Registry Number.

114837-50-2Relevant articles and documents

Synthesis of C5-allylindoles through an iridium-catalyzed asymmetric allylic substitution/oxidation reaction sequence of N-alkyl indolines

Lu, Jiamin,Xu, Ruigang,Zeng, Haixia,Zhong, Guofu,Wang, Meifang,Ni, Zhigang,Zeng, Xiaofei

supporting information, p. 3426 - 3431 (2021/05/07)

Iridium/Br?nsted acid cooperative catalyzed asymmetric allylic substitution reactions at the C5 position of indolines have been reported for the first time. The highly efficient protocol allows rapid access to various C5-allylated products in good to high

[Pd]-Catalyzedpara-selective allylation of phenols: access to 4-[(E)-3-aryl/alkylprop-2-enyl]phenols

Chinnabattigalla, Sreenivasulu,Choudhury, Aditya,Gedu, Satyanarayana

supporting information, p. 8259 - 8263 (2021/10/12)

4-[(E)-3-Arylprop-2-enyl]phenols are omnipresent scaffolds and constitute natural products and biologically significant compounds. Obtusastyrene and obtustyrene are two such phenolic-based natural products isolated fromDalbergia retusa. The development of strategies based on a site-selective allylation, particularly protecting group-free substrates and non-activated coupling agents, is indispensable in organic synthesis. Herein, we present a highly regioselective [Pd]-catalyzedpara-allylation of phenols using simple, inactivated allylic alcohols as allylating coupling partners. Notably, this strategy is successful in open-air and under mild reaction conditions. Besides, the efficacy of the present protocol was demonstrated by the direct synthesis of obtusastyrene and obtustyrene.

A Convenient Palladium-Catalyzed Carbonylative Synthesis of (E)-3-Benzylidenechroman-4-ones

Wang, Wei-Feng,Peng, Jin-Bao,Qi, Xinxin,Ying, Jun,Wu, Xiao-Feng

supporting information, p. 3521 - 3524 (2019/02/14)

A convenient palladium-catalyzed carbonylation reaction for the efficient synthesis of (E)-3-benzylidenechroman-4-ones has been developed. Using TFBen as a solid CO source, a range of substituted (E)-3-benzylidenechroman-4-ones were prepared in moderate to good yields with 2-iodophenols and allyl chlorides as the substrates. Additionally, substituted quinolin-4(1H)-ones can also be obtained with 2-iodoaniline as the starting material.

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