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4-chloro-2-methyl-6-propylpyrimidine, also known as CMP pyrimidine, is a pyrimidine derivative with a molecular formula of C8H12ClN3. It features a chloro substituent at the 4-position, a methyl group at the 2-position, and a propyl group at the 6-position. This versatile chemical compound is widely recognized for its potential applications in medicine and agriculture, particularly as an intermediate in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals.

89967-20-4

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89967-20-4 Usage

Uses

Used in Pharmaceutical Industry:
4-chloro-2-methyl-6-propylpyrimidine is used as a chemical intermediate for the synthesis of various pharmaceuticals. Its unique structure allows it to be a key component in the development of new drugs with specific therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical sector, 4-chloro-2-methyl-6-propylpyrimidine serves as an intermediate in the production of agrochemicals. Its incorporation into these products can contribute to the effectiveness of pesticides, herbicides, and other agricultural chemicals.
Used in Cancer Research:
4-chloro-2-methyl-6-propylpyrimidine is used as a potential anti-cancer agent. Its biological activities are being studied for its role in inhibiting the growth and proliferation of cancer cells, making it a promising candidate for further research and development in oncology.
Used in Protein Kinase Inhibition:
4-chloro-2-methyl-6-propylpyrimidine is also utilized in the study of protein kinase inhibition. Its potential to modulate the activity of protein kinases, which are often implicated in various diseases, positions it as a candidate for the development of targeted therapies for a range of conditions.
Overall, 4-chloro-2-methyl-6-propylpyrimidine is a multifaceted compound with a broad spectrum of applications across different industries, particularly医药 and agriculture, where it contributes to the advancement of new therapeutic agents and agrochemical products.

Check Digit Verification of cas no

The CAS Registry Mumber 89967-20-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,9,6 and 7 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 89967-20:
(7*8)+(6*9)+(5*9)+(4*6)+(3*7)+(2*2)+(1*0)=204
204 % 10 = 4
So 89967-20-4 is a valid CAS Registry Number.
InChI:InChI=1/C8H11ClN2/c1-3-4-7-5-8(9)11-6(2)10-7/h5H,3-4H2,1-2H3

89967-20-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-chloro-2-methyl-6-propylpyrimidine

1.2 Other means of identification

Product number -
Other names 4-Chlor-2-methyl-6-propylpyrimidin

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:89967-20-4 SDS

89967-20-4Relevant academic research and scientific papers

TRIAZOLOPYRIMIDINE DERIVATIVES WHICH ARE ANGIOTENSIN II RECEPTOR ANTAGONISTS

-

, (2008/06/13)

The present invention relates to the derivatives of formula: STR1 and to their tautomeric forms as well as to their addition salts and to their use in therapy, in particular for the treatment of cardiovascular diseases, especially for the treatment of hypertension, cardiac insufficiency and diseases of the arterial wall.

Studies on Pyrimidine Derivatives. XXXIII. Synthesis of Alkyl Pyrimidinyl Ketones by Means of Nitrosation of Alkylpyrimidines

Sakamoto, Takao,Sakasai, Takeji,Yoshizawa, Hiroshi,Tanji, Ken-Ichi,Nishimura, Sumiko,Yamanaka, Hiroshi

, p. 4554 - 4560 (2007/10/02)

The reaction of 4-alkylpyrimidines with propyl nitrite under acidic conditions followed by deoximation of the resulting ketoximes gave alkyl pyrimidinyl ketones in satisfactory yields.As compared with the direct oxidation of the alkylpyrimidines with sele

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