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5-BROMO-2-CHLORO-4-(METHYLTHIO)PYRIMIDINE is a heterocyclic chemical compound with the molecular formula C5H4BrClN2S. It features a pyrimidine ring structure with bromine, chlorine, and a methylthio group attached, making it a versatile building block in the synthesis of biologically active compounds.

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  • 59549-51-8 Structure
  • Basic information

    1. Product Name: 5-BROMO-2-CHLORO-4-(METHYLTHIO)PYRIMIDINE
    2. Synonyms: 5-BROMO-2-CHLORO-4-(METHYLTHIO)PYRIMIDINE;5-Bromo-2-chloro-4-(methylsulphanyl)pyrimidine;5-Bromo-2-chloro-4-(methylsulfanyl)pyrimidine;5-Bromo-2-chloro-4-(methylsulphanyl)pyrimidine, 5-Bromo-2-chloro-4-(methylthio)-1,3-diazine;5-Bromo-2-chloro-4-(methylthio)
    3. CAS NO:59549-51-8
    4. Molecular Formula: C5H4BrClN2S
    5. Molecular Weight: 239.52
    6. EINECS: N/A
    7. Product Categories: Building Blocks;Pyrimidine
    8. Mol File: 59549-51-8.mol
  • Chemical Properties

    1. Melting Point: 56-58℃
    2. Boiling Point: 346.1 °C at 760 mmHg
    3. Flash Point: 163.1 °C
    4. Appearance: /
    5. Density: 1.83
    6. Vapor Pressure: 0.000118mmHg at 25°C
    7. Refractive Index: 1.649
    8. Storage Temp.: under inert gas (nitrogen or Argon) at 2–8 °C
    9. Solubility: N/A
    10. PKA: -1.87±0.29(Predicted)
    11. CAS DataBase Reference: 5-BROMO-2-CHLORO-4-(METHYLTHIO)PYRIMIDINE(CAS DataBase Reference)
    12. NIST Chemistry Reference: 5-BROMO-2-CHLORO-4-(METHYLTHIO)PYRIMIDINE(59549-51-8)
    13. EPA Substance Registry System: 5-BROMO-2-CHLORO-4-(METHYLTHIO)PYRIMIDINE(59549-51-8)
  • Safety Data

    1. Hazard Codes: Xi
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 59549-51-8(Hazardous Substances Data)

59549-51-8 Usage

Uses

Used in Pharmaceutical Industry:
5-BROMO-2-CHLORO-4-(METHYLTHIO)PYRIMIDINE is used as a building block for the synthesis of various biologically active compounds, contributing to the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, 5-BROMO-2-CHLORO-4-(METHYLTHIO)PYRIMIDINE serves as a key component in the creation of agrochemicals, such as pesticides and herbicides, due to its ability to be incorporated into molecules with specific biological activities.
Used as a Reagent in Organic Synthesis:
5-BROMO-2-CHLORO-4-(METHYLTHIO)PYRIMIDINE is utilized as a reagent to introduce the 2-chloro-4-(methylthio)pyrimidine group into other molecules, facilitating the synthesis of diverse organic compounds with specific properties and applications.
Safety Note:
Due to its moderate toxicity, 5-BROMO-2-CHLORO-4-(METHYLTHIO)PYRIMIDINE should be handled with care in laboratory settings to ensure the safety of researchers and the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 59549-51-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,5,4 and 9 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 59549-51:
(7*5)+(6*9)+(5*5)+(4*4)+(3*9)+(2*5)+(1*1)=168
168 % 10 = 8
So 59549-51-8 is a valid CAS Registry Number.
InChI:InChI=1/C5H4BrClN2S/c1-10-4-3(6)2-8-5(7)9-4/h2H,1H3

59549-51-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-Bromo-2-chloro-4-(methylthio)pyrimidine

1.2 Other means of identification

Product number -
Other names 5-bromo-2-chloro-4-methylsulfanylpyrimidine

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:59549-51-8 SDS

59549-51-8Relevant articles and documents

JNK inhibitor as well as pharmaceutical composition and application thereof

-

Paragraph 0381-0385, (2021/03/31)

The invention provides a compound represented by a formula (I), racemates, stereoisomers, tautomers, isotope markers, solvates, polymorphic substances, nitrogen oxides, or pharmaceutically acceptablesalts thereof, and application as a JNK inhibitor. The invention also provides a preparation method of the compound shown in the formula (I), a pharmaceutical composition containing the compound shownin the formula (I), and application of the compound shown in the formula (I) to preparation of a medicine, and the medicine is used for treating diseases which can be treated by inhibiting the activity of JNK.

Substituted sulphoximines as Tie2 inhibitors and salts thereof, pharmaceutical compositions comprising the same, methods of preparing the same and uses of the same

-

Page/Page column 36, (2008/06/13)

The invention relates to substituted sulphoximines according to the general formula (I): in which A, E, G, X, R1, R2, R3, R4, R5, R6, R7, R8, m, p, q, are given in the

NOVEL HETARYL-PHENYLENEDIAMINE-PYRIMIDINES AS PROTEIN KINASE INHIBITORS

-

Page/Page column 8, (2008/12/07)

The invention relates to novel hetaryl-phenylenediamine-pyrimidines and to their structurally related oxygen and sulphur analogues of the general formula I, processes for their preparation, and their use as medicaments.

SULFOXIMINE-SUBSTITUTED PYRIMIDINES , THEIR PREPARATION AND USE AS DRUGS

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Page/Page column 252-253, (2010/11/27)

The invention relates to sulfoximine-substituted pyrimidines of the general Formula (I) processes for the preparation thereof and their use as kinase inhibitors for treating for example cancer or inflammation.

Sulfoximine-substituted pyrimidines, processes for production thereof and use thereof as drugs

-

Page/Page column 109, (2010/11/28)

The invention relates to sulfoximine-substituted pyrimidines of the general formula I processes for the preparation thereof and their use as drugs.

Syntheses and optimization of new GS39783 analogues as positive allosteric modulators of GABAB receptors

Guery, Sebastien,Floersheim, Philipp,Kaupmann, Klemens,Froestl, Wolfgang

, p. 6206 - 6211 (2008/04/03)

The optimization of GS39783 into potent, selective, and safe positive allosteric modulators of GABAB receptors is presented.

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