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3H-Pyrazol-3-one, 4-bromo-2,4-dihydro-5-methyl-2-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

41927-23-5

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41927-23-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 41927-23-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,9,2 and 7 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 41927-23:
(7*4)+(6*1)+(5*9)+(4*2)+(3*7)+(2*2)+(1*3)=115
115 % 10 = 5
So 41927-23-5 is a valid CAS Registry Number.

41927-23-5SDS

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 4-bromo-5-methyl-2-phenyl-4H-pyrazol-3-one

1.2 Other means of identification

Product number -
Other names 4-bromo-3-methyl-1-phenyl-2-pyrazolin-5-one

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:41927-23-5 SDS

41927-23-5Relevant academic research and scientific papers

Asymmetric Construction of Bispiro-Cyclopropane-Pyrazolones via a [2+1] Cyclization Reaction by Dipeptide-Based Phosphonium Salt Catalysis

Lu, Dongming,Liu, Xin,Wu, Jia-Hong,Zhang, Song,Tan, Jian-Ping,Yu, Xiaojun,Wang, Tianli

, p. 1966 - 1971 (2020)

We reported herein an efficient alternative for asymmetric synthesis of structurally complicated chiral bispiro-cyclopropane-pyrazolones via dipeptide-based phosphonium salt catalyzed [2+1] cyclization of 2,3-dioxopyrrolidines and halogenated pyrazolones. With this catalytic asymmetric protocol, a broad range of bispiro heterocyclic compounds bearing a pyrazolone unit were prepared in high yields with excellent diastereo- and enatioselectivities. Of note, this transformation proceeds in a really short time under mild reaction conditions. (Figure presented.).

Cascade assembling of pyrazolin-5-ones and benzylidenemalononitriles: The facile and efficient approach to medicinally relevant spirocyclopropylpyrazolone scaffold

Vereshchagin, Anatoly N.,Elinson, Michail N.,Korshunov, Aleksander D.,Korolev, Victor A.,Egorov, Mikhail P.

, p. 355 - 360 (2015)

A new cascade reaction provides a direct transformation of pyrazolin-5-ones and benzylidene-malononitriles by the action of bromine into substituted spirocyclopropylpyrazolones in 60-88% yields. This process can be realized in two variants, namely, (1) by treatment with bromine in the presence of base and (2) by treatment with bromine only with heating. These facile and efficient one-step cascade processes lead to the spirocyclopropylpyrazolone framework, which is present in a perspective class of compounds with prominent pharmacological and physiological activity.

With herbicidal active pyrazole ether compounds and the use thereof

-

, (2018/10/19)

The invention relates to the technical field of herbicides, and particularly discloses a pyrazole ether compound with herbicidal activity and application thereof. The pyrazole ether compound with the herbicidal activity is a general-formula compound, and the specification specifically discloses 12 kinds of compounds. An experiment result shows that the general-formula compound has high biological activity on weeds and it is hopeful that the pyrazole ether compound serves as herbicide in agriculture and other fields.

Synthesis new and novel aryl thiazole derivatives compounds

Akbarzadeh, Abolfath,Soleymani, Reza,Taheri, Milad,Ali, Maryam Karimi-Cheshmeh

, p. 153 - 164 (2012/09/07)

Six new compounds of Thiazoles family was synthesis from condensation reaction of some compounds from pyrazolines. NMR, IR and elemental analysis was used for identification of these compounds. Position of aliphatic and aromatic hydrogens in pyrazolone and thiazole cycles had established proceeding of identification. Most of obtained compounds like aciform crystals, their color is white and yellow. Reaction time and yield of these compounds had shown better results as compared with other thiazole derivations.

New synthetic methods: Part I - Regioselective 1, 2-transposition of carbonyl group in carbocyclic and heterocyclic ketones

Chande, Madhukar S.,Amle, Anand P.

, p. 2625 - 2627 (2007/10/03)

A convenient and simple synthetic method for 1, 2- transposition of keto group in pyrazol-5-ones, indan-1,3-dione and benzofuran-3-one is described.

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