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2-METHYL-4-PHENYLPYRIMIDINE, a pyrimidine derivative with the molecular formula C12H10N2, is a chemical compound featuring a pyrimidine ring with a methyl and a phenyl group attached. This unique molecular structure endows it with potential biological activity and pharmacological properties, positioning it as a promising candidate for drug design and synthesis in the pharmaceutical industry.

21203-79-2

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21203-79-2 Usage

Uses

Used in Pharmaceutical Industry:
2-METHYL-4-PHENYLPYRIMIDINE is used as a drug discovery and development candidate due to its potential biological activity and pharmacological properties. Its specific applications and effects are context-dependent, but its unique molecular structure and properties make it an interesting and potentially valuable chemical compound for research and industrial applications within this field.

Check Digit Verification of cas no

The CAS Registry Mumber 21203-79-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,2,0 and 3 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 21203-79:
(7*2)+(6*1)+(5*2)+(4*0)+(3*3)+(2*7)+(1*9)=62
62 % 10 = 2
So 21203-79-2 is a valid CAS Registry Number.

21203-79-2SDS

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 2-methyl-4-phenylpyrimidine

1.2 Other means of identification

Product number -
Other names 2-Methyl-6-phenyl-pyrimidin

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:21203-79-2 SDS

21203-79-2Relevant academic research and scientific papers

Au(I)-catalyzed domino intramolecular cyclization for the synthesis of 2,4-disubstituted pyrimidines

Zhan, Haiying,Chen, Longbin,Tan, Jingwen,Cao, Hua

, p. 109 - 112 (2016)

An efficient Au-catalyzed domino intramolecular cyclization reaction has been developed for the construction of pyrimidine derivatives from ynals and amidines at room temperature for 3 h. This transformation provides a new method for the formation of C-C

A novel and efficient lewis acid catalysed preparation of pyrimidines: Microwave-promoted reaction of urea and β-formyl enamides

Barthakur, Madan G.,Borthakur, Moyurima,Devi, Prarthana,Saikia, Chandan J.,Saikia, Anil,Bora, Utpal,Chetia, Apurba,Boruah, Romesh C.

, p. 223 - 226 (2007)

A novel and efficient synthesis of pyrimidine from β-formyl enamide is described. The key step involves samarium chloride catalysed cyclisation of β-formyl enamides using urea as source of ammonia under microwave irradiation. Georg Thieme Verlag Stuttgart

Heterogeneous gold(I)-catalyzed cyclization between ynals and amidines: An efficient and practical synthesis of 2,4-disubstituted pyrimidines

Jiang, Minhua,Nie, Quan,Cai, Mingzhong

, p. 2488 - 2500 (2019/07/12)

A novel and highly efficient heterogeneous gold(I)-catalyzed cyclization between ynals and amidines has been developed that proceeds smoothly under mild conditions and provides a general and practical method for the synthesis of a wide variety of 2,4-disu

Pyrimidine as an Aryl C-H Activating Group

Gupta, Sahaj,Melanson, Jennifer A.,Vaillancourt, Louis,Nugent, William A.,Tanoury, Gerald J.,Schatte, Gabriele,Snieckus, Victor

supporting information, p. 3745 - 3748 (2018/07/22)

The Pd-catalyzed regioselective C-H activation/arylation, /iodination, and/acetoxylation reactions of 4-arylpyrimidines using aryl iodides, N-iodosuccinimide, and (diacetoxyiodo)benzene respectively as coupling partners are described. Suzuki-Miyaura coupl

Synthesis of 4-aryl and unsymmetrical 4,6-diarylpyrimidines by the Suzuki-Miyaura cross-coupling reaction

Gupta, Sahaj,Melanson, Jennifer A.,Selim Hossain,Vaillancourt, Louis,Tanoury, Gerald J.,Nugent, William A.,Snieckus, Victor

, p. 1549 - 1569 (2018/10/04)

A two-step procedure for the synthesis of 4-arylpyrimidines from inexpensive 4,6-dichloropyrimidine via a Suzuki-Miyaura/hydrodechlorination reaction sequence is described. The reaction resulted in the predominant formation of mono-arylated product. The c

Cu-Catalyzed [3 + 3] Annulation for the Synthesis of Pyrimidines via β-C(sp3)-H Functionalization of Saturated Ketones

Zhan, Jun-Long,Wu, Meng-Wei,Chen, Fei,Han, Bing

, p. 11994 - 12000 (2016/12/09)

A novel, efficient, and facile approach for the synthesis of structurally important pyrimidines has been successfully developed by Cu-catalyzed and 4-HO-TEMPO-mediated [3 + 3] annulation of commercially available amidines with saturated ketones. This method provides a new protocol for the synthesis of pyrimidines by a cascade reaction of oxidative dehydrogenation/annulation/oxidative aromatization via direct β-C(sp3)-H functionalization of saturated ketones followed by annulation with amidines.

Transition Metal Free Intermolecular Direct Oxidative C-N Bond Formation to Polysubstituted Pyrimidines Using Molecular Oxygen as the Sole Oxidant

Guo, Wei,Li, Chunsheng,Liao, Jianhua,Ji, Fanghua,Liu, Dongqing,Wu, Wanqing,Jiang, Huanfeng

, p. 5538 - 5546 (2016/07/13)

Various polysubstituted pyrimidines are smoothly formed via a base-promoted intermolecular oxidation C-N bond formation of allylic C(sp3)-H and vinylic C(sp2)-H of allyllic compounds with amidines using O2 as the sole oxid

Base mediated direct C-H amination for pyrimidines synthesis from amidines and cinnamaldehydes using oxygen as green oxidants

Guo, Wei

, p. 47 - 50 (2016/01/25)

A direct metal-free C-H amination reaction of cinnamaldehydes and amidines to realize the synthesis of polysubstituted pyrimidines was developed in the presence of base. This greener synthetic methodology provides a straightforward approach to the synthes

Catalytic asymmetric hydrogenation of pyrimidines

Kuwano, Ryoichi,Hashiguchi, Yuta,Ikeda, Ryuhei,Ishizuka, Kentaro

supporting information, p. 2393 - 2396 (2015/03/04)

The asymmetric hydrogenation of pyrimidines proceeded with high enantioselectivity (up to 99% ee) using an iridium catalyst composed of [IrCl(cod)]2, a ferrocene-containing chiral diphosphine ligand (Josiphos), iodine, and Yb(OTf)3 (cod=1,5-cyclooctadiene). The chiral catalyst converted various 4-substituted pyrimidines into chiral 1,4,5,6-tetrahydropyrimidines in high yield. The lanthanide triflate is crucial for achieving the high enantioselectivity as well as for activating the heteroarene substrate.

Catalytic arylation of a C-H bond in pyridine and related six-membered N-heteroarenes using organozinc reagents

Hyodo, Isao,Tobisu, Mamoru,Chatani, Naoto

supporting information; experimental part, p. 1357 - 1365 (2012/08/08)

Despite significant advances in the catalytic direct arylation of heteroarenes, the application of this reaction to pyridines has been met with limited success. An oxidative nucleophilic arylation strategy has been developed to overcome this problem. Pyridine, pyrazine, quinolone, and related electron-deficient N-heteroarenes can be arylated at the most electrophilic site using the developed nickel-catalyzed reaction. This protocol serves as a complementary method to catalytic direct arylation reactions. Less is more: Pyridine, pyrazine, quinoline and related electron-deficient N-heteroarenes can be arylated at the most electrophilic site using organozinc reagents through nickel catalysis. This protocol serves as a complementary method to catalytic direct arylation reactions. Copyright

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