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Used in Pharmaceutical Industry:
1-benzyl-4-bromo-3,5-dimethyl-1H-pyrazole(SALTDATA: HCl) is used as a building block in organic synthesis for the creation of various pyrazole derivatives. These derivatives have potential applications in the development of pharmaceuticals, including drugs for the treatment of various diseases and conditions.
Used in Research Applications:
1-benzyl-4-bromo-3,5-dimethyl-1H-pyrazole(SALTDATA: HCl) is used as a research compound to study its properties and potential applications in various fields. The HCl salt form of 1-benzyl-4-bromo-3,5-dimethyl-1H-pyrazole(SALTDATA: HCl) is commonly used for its increased stability and improved properties, making it easier to handle and utilize in research settings. Additionally, the HCl salt form can also improve the solubility and bioavailability of the compound, making it more effective in biological systems for research purposes.

51108-53-3

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51108-53-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 51108-53-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,1,0 and 8 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 51108-53:
(7*5)+(6*1)+(5*1)+(4*0)+(3*8)+(2*5)+(1*3)=83
83 % 10 = 3
So 51108-53-3 is a valid CAS Registry Number.

51108-53-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-Benzyl-4-bromo-3,5-dimethyl-1H-pyrazole hydrochloride

1.2 Other means of identification

Product number -
Other names 1-benzyl-4-bromo-3,5-dimethyl-1H-pyrazole

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:51108-53-3 SDS

51108-53-3Downstream Products

51108-53-3Relevant academic research and scientific papers

A mild halogenation of pyrazoles using sodium halide salts and Oxone

Olsen, Kathryn L.,Jensen, Matthew R.,MacKay, James A.

supporting information, p. 4111 - 4114 (2017/09/29)

A mild, inexpensive, and operationally simple pyrazole halogenation method utilizing Oxone and sodium halide salts is reported. This work documents 17 examples of alkyl, aryl, allyl, and benzyl substituted 4-chloro and 4-bromopyrazoles, obtained in up to 93% yield. Reactions are performed in water under ambient conditions and generation of organic byproducts is avoided.

Rearrangement of N-(Alkylamino)azoles in Acid Media: A New Entry to C-Amino-N-substituted Azoles

Salazar, Loreto,Espada, Modesta,Avendano, Carmen,Claramunt, Rosa Maria,Sanz, Dionisia,Elguero, Jose

, p. 1563 - 1567 (2007/10/02)

A ring-opening / ring-closure mechanism for the thermal rearrangement of 1-(alkylamino)pyrazoles into 5-amino-1-alkylpyrazoles in acid medium has been established. 1-(Benzylamino)pyrazoles show a different reactivity, affording bis(5-amino-1-benzyl-4-pyrazolyl)phenylmethanes.The reaction was extended to 1-(alkylamino)indazoles but failed in the case of 1-(alkylamino)-1,2,4-triazoles.

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