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4-Amino-6-chloro-2-(methylthio)pyrimidine is a halogenated heterocycle that serves as a valuable synthesis intermediate in various chemical reactions. It is characterized by its off-white to beige or yellow crystalline powder form.

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  • 1005-38-5 Structure
  • Basic information

    1. Product Name: 4-Amino-6-chloro-2-(methylthio)pyrimidine
    2. Synonyms: 4-Pyrimidinamine, 6-chloro-2-(methylthio)-;6-Chloro-2-(methylsulfanyl)-4-pyrimidinylamine;U 8342;2-METHYLMERCAPTO-4-AMINO-AMINO-6-CHLOROPYRIMIDINE;4-AMINO-6-CHLORO-2-METHYLMERCAPTOPYRIMIDINE;4-AMINO-6-CHLORO-2-(METHYLTHIO)PYRIMIDINE;6-AMINO-4-CHLORO-2-METHYLMERCAPTOPYRIMIDINE;6-CHLORO-2-(METHYLTHIO)PYRIMIDIN-4-AMINE
    3. CAS NO:1005-38-5
    4. Molecular Formula: C5H6ClN3S
    5. Molecular Weight: 175.64
    6. EINECS: 213-734-3
    7. Product Categories: Sulphur Derivatives;Building Blocks;Halogenated Heterocycles;Heterocyclic Building Blocks;Pyrimidines;PyrimidinesHeterocyclic Building Blocks;Building Blocks;C4 to C5;Chemical Synthesis;Halogenated Heterocycles;Heterocyclic Building Blocks;Heterocycle-Pyrimidine series
    8. Mol File: 1005-38-5.mol
  • Chemical Properties

    1. Melting Point: 130-132 °C(lit.)
    2. Boiling Point: 338.7°Cat760mmHg
    3. Flash Point: 158.6°C
    4. Appearance: Off-white to beige or yellow/Crystalline Powder
    5. Density: 1.395 (estimate)
    6. Vapor Pressure: 9.64E-05mmHg at 25°C
    7. Refractive Index: 1.6100 (estimate)
    8. Storage Temp.: Keep in dark place,Sealed in dry,Room Temperature
    9. Solubility: soluble in Methanol
    10. PKA: 1.11±0.10(Predicted)
    11. CAS DataBase Reference: 4-Amino-6-chloro-2-(methylthio)pyrimidine(CAS DataBase Reference)
    12. NIST Chemistry Reference: 4-Amino-6-chloro-2-(methylthio)pyrimidine(1005-38-5)
    13. EPA Substance Registry System: 4-Amino-6-chloro-2-(methylthio)pyrimidine(1005-38-5)
  • Safety Data

    1. Hazard Codes: Xi
    2. Statements: 36/37/38
    3. Safety Statements: 37/39-26
    4. WGK Germany: 3
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 1005-38-5(Hazardous Substances Data)

1005-38-5 Usage

Uses

Used in Pharmaceutical Industry:
4-Amino-6-chloro-2-(methylthio)pyrimidine is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its unique chemical structure allows for the development of new drugs with potential therapeutic applications.
Used in Chemical Research:
As a halogenated heterocycle, 4-Amino-6-chloro-2-(methylthio)pyrimidine is utilized in chemical research for the exploration of novel reactions and the synthesis of complex organic molecules. Its versatility makes it a valuable tool for advancing scientific knowledge in the field of organic chemistry.

Synthesis Reference(s)

Journal of the American Chemical Society, 77, p. 1098, 1955 DOI: 10.1021/ja01610a006

Check Digit Verification of cas no

The CAS Registry Mumber 1005-38-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,0 and 5 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1005-38:
(6*1)+(5*0)+(4*0)+(3*5)+(2*3)+(1*8)=35
35 % 10 = 5
So 1005-38-5 is a valid CAS Registry Number.
InChI:InChI=1/C5H6ClN3S/c1-10-5-8-3(6)2-4(7)9-5/h2H,1H3,(H2,7,8,9)

1005-38-5 Well-known Company Product Price

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  • (Code)Product description
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  • Aldrich

  • (A46005)  4-Amino-6-chloro-2-(methylthio)pyrimidine  97%

  • 1005-38-5

  • A46005-5G

  • 1,306.89CNY

  • Detail
  • Aldrich

  • (A46005)  4-Amino-6-chloro-2-(methylthio)pyrimidine  97%

  • 1005-38-5

  • A46005-25G

  • 5,420.61CNY

  • Detail

1005-38-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Amino-6-chloro-2-(methylthio)pyrimidine

1.2 Other means of identification

Product number -
Other names 4-Pyrimidinamine, 6-chloro-2-(methylthio)-

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:1005-38-5 SDS

1005-38-5Relevant articles and documents

Structure-based drug design of novel, potent, and selective azabenzimidazoles (ABI) as ATR inhibitors

Barsanti, Paul A.,Pan, Yue,Lu, Yipin,Jain, Rama,Cox, Matthew,Aversa, Robert J.,Dillon, Michael P.,Elling, Robert,Hu, Cheng,Jin, Xianming,Knapp, Mark,Lan, Jiong,Ramurthy, Savithri,Rudewicz, Patrick,Setti, Lina,Subramanian, Sharadha,Mathur, Michelle,Taricani, Lorena,Thomas, George,Xiao, Linda,Yue, Qin

, p. 42 - 46 (2015)

Compound 13 was discovered through morphing of the ATR biochemical HTS hit 1. The ABI series was potent and selective for ATR. Incorporation of a 6-azaindole afforded a marked increase in cellular potency but was associated with poor PK and hERG ion channel inhibition. DMPK experiments established that CYP P450 and AO metabolism in conjunction with Pgp and BCRP efflux were major causative mechanisms for the observed PK. The series also harbored the CYP3A4 TDI liability driven by the presence of both a morpholine and an indole moiety. Incorporation of an adjacent fluorine or nitrogen into the 6-azaindole addressed many of the various medicinal chemistry issues encountered. (Chemical Presented).

New approach to synthesize symmetrical and unsymmetrical 6-(N-Alkyl(Aryl)amino)-and 6-(N, N-dialkyl(Aryl)amino)-2,4-bis(Alkyl(Aryl)Thio) pyrimidines as anti-platelet agents

Liu, Guocheng,Xu, Jiaxi,Yu, Mingwu,Chen, Ning,Zhang, Si,Ding, Zhongren,Du, Hongguang

scheme or table, p. 650 - 659 (2012/06/01)

A new and straightforward procedure has been developed for the preparation of symmetrical and unsymmetrical 6-(N-alkyl(aryl)amino)-and 6-(N,N- bisalkyl(aryl)amino)-2,4-bis(alkyl(aryl)thio)pyrimidines. The two identical or different alkylthio groups were s

THERAPEUTIC METHODS AND COMPOSITIONS INVOLVING ALLOSTERIC KINASE INHIBITION

-

Page/Page column 100-101, (2011/09/14)

The present invention is directed to methods and compositions for suppressing lymphangiogenesis, angiogenesis and/or tumor growth. The methods comprise contacting the tumor with a compound that (i) stabilizes a protein kinase in the inactive state and (ii

Novel synthesis approach and antiplatelet activity evaluation of 6-alkylamino-2,4-dialkyl(aryl)thiopyrimidines

Liu, Guocheng,Xu, Jiaxi,Park, Ki Chul,Chen, Ning,Zhang, Si,Ding, Zhongren,Wang, Feng,Du, Hongguang

experimental part, p. 5156 - 5161 (2011/07/31)

A new and efficient procedure has been designed for the preparation of 6-alkylamino-2,4-dialkyl(aryl)thiopyrimidines. The first alkylthio group was introduced into the pyrimidine ring by S-alkylation. The introduction of the second one was successfully ac

AMINOTHIAZOLE DERIVATIVES AS INHIBITORS OF MARK

-

Page/Page column 25, (2008/06/13)

Compounds of formula (I): inhibit microtubule affinity regulating kinase (MARK) and therefore find use in treatment of neurodegenerative diseases associated with hyperphosphorylation of tau.

Antitumor studies. Part 3: Design, synthesis, antitumor activity, and molecular docking study of novel 2-methylthio-, 2-amino-, and 2-(N-substituted amino)-10-alkyl-2-deoxo-5-deazaflavins

Ali, Hamed I.,Ashida, Noriyuki,Nagamatsu, Tomohisa

, p. 6336 - 6352 (2008/03/18)

Various novel 10-alkyl-2-deoxo-2-methylthio-5-deazaflavins have been synthesized by reaction of 6-(N-alkylanilino)-2-methylthiopyrimidin-4(3H)-ones with Vilsmeier reagent. The similar 2-(N-substituted amino) derivatives were prepared by nucleophilic replacement reaction of the 2-methylthio moiety by appropriate amines. The 2-oxo derivatives (i.e., 5-deazaflavins) were obtained by acidic hydrolysis of the 2-methylthio derivatives. The antitumor activities against CCRF-HSB-2 and KB cells and the antiviral activities against HSV-1 and HSV-2 have been investigated in vitro, and many compounds showed promising antitumor activities. Furthermore, AutoDock molecular docking into PTK has been done for lead optimization of these compounds as potential PTK inhibitors. Whereas, the designed 2-deoxo-5-deazaflavins connected with amino acids at the 2-position exhibited the good binding affinities into PTK with more hydrogen bonds.

Substituted heterocyclic compounds and methods of use

-

Page/Page column 20, (2008/06/13)

The present invention relates to triazolopyrimidines, imidazolopyrimidines and derivatives thereof, and pharmaceutically acceptable salts thereof. Also included is a method of treatment of inflammation, rheumatoid arthritis, Pagets disease, osteoporosis,

Solid-phase synthesis of 2,4,6-triaminopyrimidines

Guillier, Fabrice,Roussel, Patrick,Moser, Heinz,Kane, Peter,Bradley, Mark

, p. 3450 - 3458 (2007/10/03)

Substituted pyrimidines are an important class of kinase inhibitors. We therefore developed a synthetic route suitable for the solid-phase synthesis of 2,4,6-triaminopyrimidines through displacement reactions on deactivated pyrimidines. Functionalising th

Antifungal method, formulations and compounds

-

, (2008/06/13)

Some known 4-amino-6-chloro-5-(H or CH3)-2-(methylthio or methoxy)pyrimidines have been found to be active against fungi. The compounds are systemically active in plants, that is to say, the compounds are carried by plant juices to sites of inf

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