What is the 1,2-Dimethyl-1,4,5,6-tetrahydropyrimidine?

1,2-Dimethyl-1,4,5,6-tetrahydropyrimidine is Slight yellow to colorless, while it's Molecular Formula is C6H12N2. Slight yellow to colorless 1,2-Dimethyl-1,4,5,6-tetrahydropyrimidine is a reagent used in the synthesis of pyrantel derivatives with nematocidal activity. Also used as a reactant in the preparation of hapten antibodies that evoke terpenoid cyclization.

What is the CAS number for 1,2-Dimethyl-1,4,5,6-tetrahydropyrimidine?

The CAS number of 1,2-Dimethyl-1,4,5,6-tetrahydropyrimidine is 4271-96-9.

What is 1,2-Dimethyl-1,4,5,6-tetrahydropyrimidine (4271-96-9) used for?

1,2-Dimethyl-1,4,5,6-tetrahydropyrimidine is an organic compound belonging to the class of pyrimidines, which are heterocyclic compounds with a six-membered ring containing four nitrogen atoms. This specific compound is characterized by the presence of two methyl groups attached to the first and second carbon atoms of the ring, making it a derivative of tetrahydropyrimidine. It is a versatile reagent in the field of organic synthesis and has potential applications in various industries due to its unique chemical properties.InChI:InChI=1/C6H12N2/c1-6-7-4-3-5-8(6)2/h3-5H2,1-2H3

What is the 1,2-Dimethyl-1,4,5,6-tetrahydropyrimidine?

1,2-Dimethyl-1,4,5,6-tetrahydropyrimidine is Slight yellow to colorless, while it's Molecular Formula is C6H12N2. Slight yellow to colorless 1,2-Dimethyl-1,4,5,6-tetrahydropyrimidine is a reagent used in the synthesis of pyrantel derivatives with nematocidal activity. Also used as a reactant in the preparation of hapten antibodies that evoke terpenoid cyclization.

What is the CAS number for 1,2-Dimethyl-1,4,5,6-tetrahydropyrimidine?

The CAS number of 1,2-Dimethyl-1,4,5,6-tetrahydropyrimidine is 4271-96-9.

What is 1,2-Dimethyl-1,4,5,6-tetrahydropyrimidine (4271-96-9) used for?

1,2-Dimethyl-1,4,5,6-tetrahydropyrimidine is an organic compound belonging to the class of pyrimidines, which are heterocyclic compounds with a six-membered ring containing four nitrogen atoms. This specific compound is characterized by the presence of two methyl groups attached to the first and second carbon atoms of the ring, making it a derivative of tetrahydropyrimidine. It is a versatile reagent in the field of organic synthesis and has potential applications in various industries due to its unique chemical properties.InChI:InChI=1/C6H12N2/c1-6-7-4-3-5-8(6)2/h3-5H2,1-2H3

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1,2-Dimethyl-1,4,5,6-Tetrahydropyrimidine supplier in China CAS NO.4271-96-9

Product Name: 1,2-Dimethyl-1,4,5,6-Tetrahydropyrimidine supplier in China CAS NO.4271-96-9
CasNo: 4271-96-9
Purity:
Appearance: Slight yellow to colorless

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Product Details

CasNo： 4271-96-9

Molecular Formula： C₆H₁₂N₂

Appearance： Slight yellow to colorless

Manufacturer supply good quality 1,2-Dimethyl-1,4,5,6-Tetrahydropyrimidine supplier in China CAS NO.4271-96-9 4271-96-9 with stock

Molecular Formula:C6H12N2
Molecular Weight:112.175
Appearance/Colour:Slight yellow to colorless
Vapor Pressure:0.507mmHg at 25°C
Refractive Index:1.513
Boiling Point:191.7 °C at 760 mmHg
PKA:13.42±0.20(Predicted)
Flash Point:69.8 °C
PSA：15.60000
Density:0.98 g/cm³
LogP:0.11380

1,2-Dimethyl-1,4,5,6-tetrahydropyrimidine(Cas 4271-96-9) Usage

InChI:InChI=1/C6H12N2/c1-6-7-4-3-5-8(6)2/h3-5H2,1-2H3

4271-96-9 Relevant articles

Synthesis and menatocidal activities of arylvinyltetrahydropyrimidines

Kraouti,Caujolle,Labidalle,Payard,Bories,Loiseau,Gayral

, p. 979 - 982 (1993)

Economical synthetic method 1, 2 - dimethyl -1, 4, 5, 6 - tetrahydropyrimidine (by machine translation)

-

Paragraph 0036-0045, (2019/09/14)

1, 2 - Dimethyl -1, 4, 5, 6 - tetrahydro...

Synthesis method of 1,2-dimethyl-1,4,5,6-tetrahydropyrimidine

-

Paragraph 0025; 0028; 0031; 0032; 0037; 0042; 0047-0057, (2018/11/27)

The invention discloses a synthesis meth...

Cyclic and linear amidine catalysts for the efficient synthesis of cyclic trithiocarbonates from carbon disulfide and episulfides under mild conditions

Aoyagi, Naoto,Endo, Takeshi

, p. 1702 - 1704 (2018/04/10)

Cyclic and linear amidines effectively c...

Push-pull alkenes by reacting N,N′-dimethyl cyclic ketene N,N′-acetals with isocyanates: synthesis, structures, and reactivities

Ye, Guozhong,Henry, William P.,Chen, Chunlong,Zhou, Aihua,Pittman Jr., Charles U.

supporting information; experimental part, p. 2135 - 2139 (2009/07/26)

N,N′-Dimethyl cyclic ketene N,N′-acetals...

4271-96-9 Process route

: 61327-70-6
1,2-dimethyl-hexahydro-pyrimidine

: 4271-96-9
1,2-dimethyl-1,4,5,6-tetrahydropyrimidine

Conditions

Conditions	Yield
With oxygen; gold; In acetonitrile; at 60 ℃; for 40h; under 760.051 Torr;	97%

: 75-05-8,26809-02-9
acetonitrile

: 6291-84-5
N-Methyl-1,3-propanediamine

: 4271-96-9
1,2-dimethyl-1,4,5,6-tetrahydropyrimidine

Conditions

Conditions	Yield
With thioacetamide; at 90 - 110 ℃; for 6h; Temperature; Reagent/catalyst; Large scale;	96%
acetonitrile; N-Methyl-1,3-propanediamine; With zinc(II) chloride; for 24h; Inert atmosphere; Reflux; Inert atmosphere;	45%

4271-96-9 Upstream products

2208-07-3
ethyl acetimidate hydrochloride
6291-84-5
N-Methyl-1,3-propanediamine
61327-70-6
1,2-dimethyl-hexahydro-pyrimidine
75-05-8
acetonitrile

4271-96-9 Downstream products

83467-04-3
1-methyl-2-(thio-p-toluoyl methylene)hexahydropyrimidine
83467-06-5
1-methyl-2-(4-nitrothiobenzoyl methylene)hexahydropyrimidine
83467-03-2
1-methyl-2-(thiobenzoyl methylene)hexahydropyrimidine
83467-05-4
1-methyl-2-(4-methoxythiobenzoyl methylene)hexahydropyrimidine

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