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2,4-Dichloro-6-methoxypyrimidine is an organic compound that serves as a crucial intermediate in the synthesis of various pharmaceutical compounds. It is characterized by its chemical structure, which includes two chlorine atoms at the 2nd and 4th positions, a methoxy group at the 6th position, and a pyrimidine ring. This structure endows it with unique properties that make it valuable in the development of certain drugs.

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  • 43212-41-5 Structure
  • Basic information

    1. Product Name: 2,4-Dichloro-6-methoxypyrimidine
    2. Synonyms: 2,4-Dichloro-6-methoxypyrimidine;2,4-Dichloro-6-methoxy-1,3-diazine;2,6-Dichloro-4-methoxypyrimidine
    3. CAS NO:43212-41-5
    4. Molecular Formula: C5H4Cl2N2O
    5. Molecular Weight: 179.01
    6. EINECS: N/A
    7. Product Categories: Heterocycle-Pyrimidine series
    8. Mol File: 43212-41-5.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 263.2±20.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.446±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
    8. Solubility: N/A
    9. PKA: -4.54±0.30(Predicted)
    10. CAS DataBase Reference: 2,4-Dichloro-6-methoxypyrimidine(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2,4-Dichloro-6-methoxypyrimidine(43212-41-5)
    12. EPA Substance Registry System: 2,4-Dichloro-6-methoxypyrimidine(43212-41-5)
  • Safety Data

    1. Hazard Codes: Xn
    2. Statements: 22-36
    3. Safety Statements: 26
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 43212-41-5(Hazardous Substances Data)

43212-41-5 Usage

Uses

Used in Pharmaceutical Industry:
2,4-Dichloro-6-methoxypyrimidine is used as a chemical intermediate for the preparation of piperazinyl pyrimidine derivatives. These derivatives act as γ-secretase modulators, which are important in the treatment of various neurodegenerative diseases, such as Alzheimer's disease. 2,4-Dichloro-6-methoxypyrimidine's role in the synthesis of these modulators is crucial for developing effective therapies against such conditions.
Additionally, 2,4-Dichloro-6-methoxypyrimidine is used in the synthesis of α-azinylalkylamino-substituted (thiazolylamino)pyrimidines and -pyrazines. These compounds are selective JAK2 inhibitors, which have potential applications in the treatment of various inflammatory and autoimmune diseases, as well as certain types of cancer. 2,4-Dichloro-6-methoxypyrimidine's involvement in the creation of these inhibitors highlights its significance in the development of targeted therapies for a range of medical conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 43212-41-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,3,2,1 and 2 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 43212-41:
(7*4)+(6*3)+(5*2)+(4*1)+(3*2)+(2*4)+(1*1)=75
75 % 10 = 5
So 43212-41-5 is a valid CAS Registry Number.

43212-41-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4-Dichloro-6-methoxypyrimidine

1.2 Other means of identification

Product number -
Other names 2,4-dichloro-6-methoxy-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:43212-41-5 SDS

43212-41-5Relevant articles and documents

HEPATITIS B VIRAL ASSEMBLY EFFECTORS

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Paragraph 00162, (2016/10/31)

Novel assembly effector compounds having a therapeutic effect against hepatitis B viral (HBV) infection are disclosed. Assembly effector molecules described herein can lead to defective viral assembly and also may affect other viral activities associated with chronic HBV infection. Also disclosed is a process to synthesize disclosed compounds, method of treatment of HBV by administration of disclosed compounds, and use of these compounds in the manufacture of medicaments against HBV.

NOVEL PYRIMIDINE DERIVATIVES, PREPARATION THEREOF, AND PHARMACEUTICAL USE THEREOF AS AKT(PKB) PHOSPHORYLATION INHIBITORS

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Paragraph 1615-1618, (2013/10/22)

The present invention relates to novel chemical compounds derived from pyrimidines, to the method for preparing same, to the novel intermediates obtained, to the use thereof as drugs, to the pharmaceutical compositions containing same, and to the therapeutic use thereof as AKT inhibitors.

Development of an efficient, scalable route for the preparation of a novel insulin-like growth factor-1 receptor modulator

Kumar, C.H. Vinod,Kavitake, Santosh,Kumar, Sythana Suresh,Cornwall, Philip,Ashok, Mithun,Bhagat, Sagar,Manjunatha, Sulur G.,Nambiar, Sudhir

, p. 1416 - 1421 (2012/10/29)

A chromatography-free and efficient synthesis of insulin-like growth factor-1 receptor (IGF-1R) modulator is reported. Herein we describe an improved synthesis for the target compound, which features facile introduction of a novel pyrrolidinyl-pyrimidyl isoxazole 8, via in situ sulfone displacement by fluorine. The overall process consists of six chemical steps and five isolations, with introduction of the expensive triheterocyclic unit 8 towards the end of the synthesis.

Replacement of pyrazol-3-yl amine hinge binder with thiazol-2-yl amine: Discovery of potent and selective JAK2 inhibitors

Ioannidis, Stephanos,Lamb, Michelle L.,Almeida, Lynsie,Guan, Huiping,Peng, Bo,Bebernitz, Geraldine,Bell, Kirsten,Alimzhanov, Marat,Zinda, Michael

scheme or table, p. 1669 - 1673 (2010/08/20)

Thiazol-2-yl amine was identified as an isosteric replacement for pyrazol-3-yl amine during our efforts to identify potent and selective JAK2 inhibitors. The rationale, synthesis and biological evaluation of several analogs is reported, along with the in vivo evaluation of the lead compounds.

AMINO-THIAZOLYL- PYRIMIDINE DERIVATIVES AND THEIR USE FOR THE TREATMENT OF CANCER

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Page/Page column 57-58, (2009/01/20)

The present invention relates to compounds of Formula (I): and to their pharmaceutical compositions, and to their methods of use. These compounds provide a treatment for myeloproliferative disorders and cancer.

S-6-METH0XY-2- (2- (3- (PYRIMID-2-YL) IS0XAZ0L-5-YL) PYRROLIDIN-1-YL) -4- (5-METHYL-IH-PYRAZOL-S-YLAMINO) PYRIMIDINE AND POLYMORPHIC FORMS THEREOF AS MODULATORS OF THE INSULIN-LIKE GROWTH

-

Page/Page column 29, (2008/12/04)

There is provided novel pyrimidine derivatives of formula (I) or pharmaceutically acceptable salsts thereof, processes for their preparation, pharmaceutical compositions containing them and their use in therapy.

PYRIMIDINE DERIVATIVES FOR THE INHIBITION OF IGF-IR TYROSINE KINASE ACTIVITY

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Page/Page column 96, (2008/06/13)

A compound of formula (I) wherein the substituents are as defined in the text for use in inhibiting insulin-like growth factor 1 receptor activity in a warm blooded animal such as man.

4-(PYRID-2-YL) AMINO SUBSTITUTED PYRIMIDINE AS PROTEIN KINASE INHIBITORS

-

Page/Page column 97, (2008/06/13)

A compound of formula (I): wherein the substituents are as defined in the text for use in inhibiting insulin-like growth factor 1 receptor activity in a warm-blooded animal such as man.

Amines useful in producing pharmaceutically active CNS compounds

-

, (2008/06/13)

Disclosed are Δ9(11) -steroids (VI) and amino substituted steroids (XI) which contain an amino group attached to the terminal carbon atom of the C17 -side chain, more particularly amino steroids (Ia and Ib), aromatic steroids (II), Δ16 -steroids (IIIa and IIIb), reduced A-ring steroids (IV), Δ17(20) -steroids (Va and Vb) and Δ9(11) -steroids (VI) which are useful as pharmaceutical agents for treating a number of conditions.

Amines useful in producing pharmaceutically active CNS compounds

-

, (2008/06/13)

Disclosed are Δ9(11) -steroids (VI) and amino substituted steroids (XI) which contain an amino group attached to the terminal carbon atom of the C17 -side chain, more particularly amino steroids (Ia and Ib), aromatic steroids (II), Δ16 -steroids (IIIa and IIIb), reduced A-ring steroids (IV), Δ17(20) -steroids (Va and Vb) and Δ9(11) -steroids (VI) which are useful as pharmaceutical agents for treating a number of conditions.

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