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[6-Methoxy-2-(4-methoxy-phenyl)-pyrimidin-4-yl]-methanol is a complex organic compound characterized by its unique molecular structure. It features a pyrimidin-4-yl core, which is a heterocyclic aromatic ring system containing two nitrogen atoms. This core is substituted with a methoxy group at the 6th position and a 4-methoxy-phenyl group at the 2nd position, which adds to the molecule's complexity. The 4-methoxy-phenyl group itself is a phenyl ring with a methoxy substituent at the 4th position, enhancing the molecule's electron-donating properties. The molecule is further functionalized with a hydroxymethyl group, which is a hydroxyl group (-OH) attached to a methyl group (-CH2), making it a methanol derivative. [6-Methoxy-2-(4-methoxy-phenyl)-pyrimidin-4-yl]-methanol is of interest in the field of organic chemistry, potentially for its pharmaceutical or chemical properties, although specific applications are not detailed in this summary.

99141-46-5

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99141-46-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 99141-46-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,1,4 and 1 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 99141-46:
(7*9)+(6*9)+(5*1)+(4*4)+(3*1)+(2*4)+(1*6)=155
155 % 10 = 5
So 99141-46-5 is a valid CAS Registry Number.

99141-46-5Downstream Products

99141-46-5Relevant academic research and scientific papers

Ring-transformation of 1,2,4-Oxadiazines. Raney Nickel Hydrogenation of Z-3-Aryl-5,6-dihydro-5-(substituted)methylene-4H-1,2,4-oxadiazine Derivatives

Tabei, Katsumi,Kawashima, Etsuko,Takada, Toyozo,Kato, Tetsuzo

, p. 569 - 574 (2007/10/02)

Raney nickel hydrogenation of Z-3-aryl-5-(ethoxycarbonyl)methylene-5,6-dihydro-4H-1,2,4-oxadiazine (1a-c) affords 2-aryl-6-hydroxymethyl-4-pyrimidinone (2) and ethyl (2-aryl-4-oxazolyl)acetate (3).A similar hydrogenation of Z-5-(arylcarbamoyl)methylene-5,

RING-TRANSFORMATION OF 1,2,4-OXADIAZINE DERIVATIVES INTO 4-HYDROXYPYRIMIDINE DERIVATIVES: CATALYTIC HYDROGENATION OF 3-ARYL-5-ETHOXYCARBONYLMETHYLENE-5,6-DIHYDRO-4H-1,2,4-OXADIAZINE DERIVATIVES

Tabei, Katsumi,Kawashima, Etsuko,Takada, Toyozo,Kato, Tetsuzo

, p. 2061 - 2066 (2007/10/02)

Catalytic hydrogenation of 3-aryl-5-ethoxycarbonylmethylene-5,6-dihydro-4H-1,2,4-oxadiazine derivatives (1) is described.The method leads to new synthesis of 2-aryl-4-hydroxypyrimidine derivatives (3) involving cyclization of ethyl 3-benzimidoylimino-4-hydroxybutanoate derivatives (2) by the elimination of ethanol.Nickel catalyzed hydrogenation of 1 gave ethyl 2-aryl-4-oxazoylacetate (4) as a by-product besides product 3.

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