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2(1H)-Pyrimidinone, 5-acetyl-3,4-dihydro-4-(2-hydroxyphenyl)-6-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

100795-75-3

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100795-75-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 100795-75-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,7,9 and 5 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 100795-75:
(8*1)+(7*0)+(6*0)+(5*7)+(4*9)+(3*5)+(2*7)+(1*5)=113
113 % 10 = 3
So 100795-75-3 is a valid CAS Registry Number.

100795-75-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(2-hydroxyphenyl)-5-acetyl-2-oxo-6-methyl-1,2,3,4-tetrahydropyrimidine

1.2 Other means of identification

Product number -
Other names 5-acetyl-4-(2-hydroxyphenyl)-6-methyl-3,4-dihydropyrimidin-2(1H)-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:100795-75-3 SDS

100795-75-3Downstream Products

100795-75-3Relevant academic research and scientific papers

Coumarin-chalcone hybrids targeting insulin receptor: Design, synthesis, anti-diabetic activity, and molecular docking

Danduga, Ravi Chandra Sekhara Reddy,Kola, Phani Kumar,Konidala, Sathish Kumar,Kotra, Vijay

, (2020)

Four series of thirteen new coumarin-chalcone hybrids (DPCU 1–13, DPCT 1–13, DCCU 1–13 and DCCT 1–13) were designed and synthesized using Biginelli synthesis, Pechmann condensation, Acetylation, and Claisen-Schmidt reactions. Synthesized compounds were te

Exploiting silver trifluoromethanesulfonate as efficient and reusable catalyst for the synthesis of dihydropyrimidine derivatives under different reaction environments

Roy, Dipak Kumar,Tamuli, Kashyap Jyoti,Bordoloi, Manobjyoti

, p. 3313 - 3323 (2019)

Different results were generated under different reaction conditions for the multicomponent reactions. Herein, an efficiently improved and mild protocol for the synthesis of dihydropyrimidine derivatives using cheap silver trifluoromethanesulfonate (CFsu

Dihydropyrimidones: A ligands urease recognition study and mechanistic insight through in vitro and in silico approach

Khan, Farman Ali,Shamim, Shahbaz,Ullah, Nisar,Lodhi, Muhammad Arif,Khan, Khalid Mohammed,Kanwal,Ali, Farman,Afridi, Sahib Gul,Perveen, Shahnaz,Khan, Ajmal

, p. 120 - 132 (2021)

Scaffold varied dihydropyrimidone derivatives 1–20 were evaluated for their selective urease inhibitory kinetics potential. Compounds 1, 2, 3, 4, 5, 6, and 12 were found to be the most promising urease inhibitors and showed the inhibition (Ki v

Fe3O4@Silica sulfuric acid core-shell composite as a novel nanomagnetic solid acid: Synthesis, characterization and application as an efficient and reusable catalyst for one-pot synthesis of 3,4-dihydropyrimidinones/thiones under sol

Kiasat, Ali Reza,Davarpanah, Jamal

, p. 2991 - 3001 (2015)

Abstract A simple and convenient method was used to prepare Fe3O4@Silica sulfuric acid core-shell composite using Fe3O4 spheres as the core and silica sulfuric acid nanoparticles as the shell. Magnetite nanopart

One-pot Synthesis of 3,4-Dihydropyrimidin-2(1H)-ones Catalysed by Cupric Acetate under Solvent-free Conditions

Kathing, Chingrishon,Rani, Jims World Star,Singh, Nongthombam Geetmani,Tumtin, Shokip,Nongrum, Ridaphun,Nongkhlaw, Rishanlang

, p. 1254 - 1258 (2014)

A solvent-free synthesis of 3,4-dihydropyrimidin-2(1H)-ones from aromatic aldehydes, β-keto ester/acetyl acetone and urea catalysed by cupric acetate under thermal condition is reported as a simple and an efficient protocol. Compared with classical Bigine

Sustainable synthetic approaches using [C16Im][Oxa] as a flexible organocatalyst and DFT studies toward 3,4-dihydropyrimidinones and benzoxazines

Y?ld?r?m, Ayhan,Kaya, Yunus

, p. 1085 - 1094 (2017)

Abstract: Easily accessible 1-hexadecyl-1H-imidazol-3-ium oxalate is highly efficient Br?nsted type acidic catalyst for the selected multicomponent one-pot reactions. The short reaction times, easy workup procedures, and green metal-free conditions for th

Synthesis and characterization of nano acid catalyst derived from rice husk silica and its application for the synthesis of 3,4-dihydropyrimidinones/thiones compounds

Davarpanah, Jamal,Sayahi, Mohammad Hosein,Ghahremani, Mahboubeh,Karkhoei, Sahar

, p. 546 - 555 (2019)

In the present work, the extraction of silica nanoparticles from the rice husk followed by the modification using an acidic ionic liquid containing imidazolium butyl sulfonic acid through a sol-gel method (RH@[SiPrImBuSO3H]Cl) has been investig

Air-stable zirconocene bis(perfluorobutanesulfonate) as a highly efficient catalyst for synthesis of N-heterocyclic compounds

Wang, Jinying,Li, Ningbo,Qiu, Renhua,Zhang, Xiaohong,Xu, Xinhua,Yin, Shuang-Feng

, p. 61 - 67 (2015)

Zirconocene bis(perfluorobutanesulfonate) is air- and water-stable and proved to be ionic on basis of conductivity measurements. It exhibits high catalytic efficiency for the synthesis of N-heterocyclic compounds under solvent-free condition, such as benzimidazoles, benzodiazepines, dihydropyrimidinones and dihydropyridines under mild condition. Furthermore, it can be reused without loss of activity in a test of five cycles. This catalytic system affords a simple and efficient approach for the synthesis of N-heterocyclic compounds.

Ultrasound-mediated synthesis of 3,4-dihydropyrimidin-2-(1H)-ones (or Thiones) with NaHSO4·H 2O

Dilmaghani, Karim Akbari,Zeynizadeh, Behzad,Amirpoor, Maryam

, p. 1634 - 1642 (2013)

A fast and efficient Biginelli synthesis of 3,4-dihydropyrimidin-2-(1H)- ones (or thiones) by the reaction of aromatic aldehydes, β-dicarbonyls, and urea/thiourea using NaHSO4·H2O/ultrasound system is presented. The reactions were ca

BiVO4-NPs: an efficient nano-catalyst for the synthesis of biscoumarins, bis(indolyl)methanes and 3,4-dihydropyrimidin-2(1H)-ones (thiones) derivatives

Shirini, Farhad,Lati, Monireh Pourghasemi

, p. 75 - 87 (2017/01/05)

BiVO4-NPs can be used as an efficient and reusable nano-catalyst for the promotion of the synthesis of biscoumarins, bis(indolyl)methanes and 3,4-dihydropyrimidin-2(1H)-ones (thiones) derivatives. The structures of the products were characteriz

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