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3,4-DIHYDRO-6-METHYL-4-OXO-2-PYRIMIDINEPROPANOIC ACID is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

86454-07-1

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86454-07-1 Usage

Synthesis Reference(s)

Journal of Heterocyclic Chemistry, 20, p. 87, 1983 DOI: 10.1002/jhet.5570200120

Check Digit Verification of cas no

The CAS Registry Mumber 86454-07-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,4,5 and 4 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 86454-07:
(7*8)+(6*6)+(5*4)+(4*5)+(3*4)+(2*0)+(1*7)=151
151 % 10 = 1
So 86454-07-1 is a valid CAS Registry Number.

86454-07-1SDS

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 3-(6-methyl-4-oxo-1H-pyrimidin-2-yl)propanoic acid

1.2 Other means of identification

Product number -
Other names 2-Pyrimidinepropanoicacid,1,6-dihydro-4-methyl-6-oxo

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:86454-07-1 SDS

86454-07-1Downstream Products

86454-07-1Relevant academic research and scientific papers

Reaction of β-Aminocrotonamide with Dibasic Acid Derivatives

Sato, Masayuki,Ogasawara, Hiromichi,Kato, Tetsuzo

, p. 87 - 91 (2007/10/02)

Reaction of β-aminocrotonamide (1) with succinic anhydride gave β-succinamidocrotonamide (3a), which was treated with base to cyclize to 3,4-dihydro-6-methyl-4-oxo-2-pyrimidinepropanoic acid (4a).Similarly, pyrimidinepentanoic acid derivative 4b was prepared from compound 1 and glutaric anhydride.Reaction of compound 1 with dimethyl succinate in the presence of sodium methoxide gave the pyrimidine derivative 4a.Similar reaction of compound 1 with glutarate, adipate, and phthalate gave the corresponding pyrimidines 4b, 4c and 4d, while reaction of compound 1 with malon ate gave 2-hydroxypyridine derivative 11 and dimethylpyrimidinone 4e.Reaction of dimethyl fumarate with compound 1 in the presence of methoxide gave a poor yield of pyrrolopyridine derivative 13.

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