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2,4-BIS(DIMETHYLAMINO)-PYRIMIDINE, a chemical compound with the molecular formula C8H14N4, is a yellow solid known for its versatile applications across various industries. It is primarily used in the synthesis of organic compounds and pharmaceuticals, serving as a reagent in chemical reactions for the production of dye intermediates, agrochemicals, and pharmaceutical raw materials. Its properties make it a valuable component in the pharmaceutical, agricultural, and chemical sectors, and it has also been studied for its potential in medicinal chemistry due to its pharmacological activities.

1076-94-4

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1076-94-4 Usage

Uses

Used in Pharmaceutical Industry:
2,4-BIS(DIMETHYLAMINO)-PYRIMIDINE is used as a reagent in the synthesis of pharmaceutical raw materials for its ability to facilitate the production of various organic compounds and pharmaceuticals.
Used in Chemical Industry:
2,4-BIS(DIMETHYLAMINO)-PYRIMIDINE is used as a reagent in chemical reactions for the production of dye intermediates, highlighting its role in the creation of colorants for various applications.
Used in Agricultural Industry:
2,4-BIS(DIMETHYLAMINO)-PYRIMIDINE is used in the synthesis of agrochemicals, contributing to the development of products that aid in crop protection and enhancement of agricultural yields.
Used in Medicinal Chemistry Research:
2,4-BIS(DIMETHYLAMINO)-PYRIMIDINE is utilized in research for its potential applications in medicinal chemistry, given its pharmacological activities that warrant further exploration for therapeutic uses.

Check Digit Verification of cas no

The CAS Registry Mumber 1076-94-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,7 and 6 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1076-94:
(6*1)+(5*0)+(4*7)+(3*6)+(2*9)+(1*4)=74
74 % 10 = 4
So 1076-94-4 is a valid CAS Registry Number.
InChI:InChI=1/C8H14N4/c1-11(2)7-5-6-9-8(10-7)12(3)4/h5-6H,1-4H3

1076-94-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-N,2-N,4-N,4-N-tetramethylpyrimidine-2,4-diamine

1.2 Other means of identification

Product number -
Other names 2,6-Bis(dimethylamino)pyrimidine

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:1076-94-4 SDS

1076-94-4Downstream Products

1076-94-4Relevant academic research and scientific papers

1-Chloro-1,3-bis(dimethylamino)-2-azapropenylium Salts: Intermediates for the Synthesis of 1,3,5-Triazines, Pyrimidines, Isoquinolines, Quinazolines, and a 1,3,5-Thiadiazinium Salt

Boyd, Gerhard V.,Lindley, Peter F.,Nicolaou, George A.

, p. 1105 - 1107 (1984)

The title salts, which are formed by the action of dimethylcyanamide on the phosphorus oxychloride complexes of a variety of tertiary amides, are useful precursors of six-membered heteroaromatic compounds: they react with simple amidines to yield 1,3,5-triazines and with N,N-dimethylamidines to give pyrimidines; 3-arylmethyl-1-chloro-1,3-bis(dimethylamino)-2-azapropenylium perchlorates form isoquinolines, the related 3-arylamino-1-chloro-1-dimethylamino-2-azapropenylium salts cyclise to quinazolinium salts, and treatment of 1-chloro-1,3-bis(dimethylamino)-3-phenyl-2-azapropenylium perchlorate with potassium thiocyanate results in a rearranged 1,3,5-thiadiazinium salt.

Convenient dimethylamino amination in heterocycles and aromatics with dimethylformamide

Agarwal, Anu,Chauhan, Prem M. S.

, p. 2925 - 2930 (2007/10/03)

A convenient dimethylamino amination of various heterocyclic and aromatic compounds having activated chloro group has been carried out in good yields using dimethyl formamide (DMF).

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