Cas no 1312535-79-7 (1-(2-Chloropyrimidin-4-yl)ethanol)

1-(2-Chloropyrimidin-4-yl)ethanol is a versatile pyrimidine derivative with significant utility in pharmaceutical and agrochemical synthesis. Its chloropyrimidine core provides a reactive site for nucleophilic substitution, enabling further functionalization, while the hydroxyl group offers additional modification potential. This compound is particularly valuable as an intermediate in the development of active pharmaceutical ingredients (APIs) and specialty chemicals. Its well-defined structure and high purity make it suitable for precision applications in medicinal chemistry and material science. The presence of both chloro and hydroxyl substituents enhances its reactivity, facilitating diverse synthetic pathways. Proper handling and storage under inert conditions are recommended to maintain stability.

1-(2-Chloropyrimidin-4-yl)ethanol structure

1312535-79-7 structure

Product Name:1-(2-Chloropyrimidin-4-yl)ethanol

CAS No:1312535-79-7

MF:C₆H₇ClN₂O

MW:158.58558011055

MDL:MFCD26403247

CID:2119961

Update Time:2025-10-23

1-(2-Chloropyrimidin-4-yl)ethanol Chemical and Physical Properties

Names and Identifiers

- 1-(2-chloropyrimidin-4-yl)ethanol
- MIUDYNZFUBDJPT-UHFFFAOYSA-N
- 4-Pyrimidinemethanol, 2-chloro-?-methyl-
- 4-Pyrimidinemethanol, 2-chloro-alpha-methyl-
- 1-(2-Chloropyrimidin-4-yl)ethanol
- MDL： MFCD26403247
- Inchi： 1S/C6H7ClN2O/c1-4(10)5-2-3-8-6(7)9-5/h2-4,10H,1H3
- InChI Key： MIUDYNZFUBDJPT-UHFFFAOYSA-N
- SMILES： ClC1=NC=CC(C(C)O)=N1

Computed Properties

Hydrogen Bond Donor Count: 1
Hydrogen Bond Acceptor Count: 3
Heavy Atom Count: 10
Rotatable Bond Count: 1
Complexity: 112
Topological Polar Surface Area: 46

1-(2-Chloropyrimidin-4-yl)ethanol Pricemore >>

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Chemenu	CM325423-1g	1-(2-chloropyrimidin-4-yl)ethanol	1312535-79-7	95%+	1g	$627	2024-08-02
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eNovation Chemicals LLC	D910201-1g	1-(2-Chloro-4-pyrimidinyl)ethanol	1312535-79-7	95%	1g	$935	2025-02-21
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1-(2-Chloropyrimidin-4-yl)ethanol Suppliers

Amadis Chemical Company Limited

Gold Member

Audited Supplier

(CAS:1312535-79-7)1-(2-Chloropyrimidin-4-yl)ethanol

Order Number:A1050254

Stock Status:in Stock

Quantity:5g

Purity:99%

Pricing Information Last Updated:Thursday, 29 August 2024 17:30

Price ($):1268.0

Email:[email protected]

Product Official Link

1-(2-Chloropyrimidin-4-yl)ethanol Related Literature

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J. Matthew Kurley,Phillip W. Halstenberg,Abbey McAlister,Stephen Raiman,Richard T. Mayes RSC Adv., 2019,9, 25602-25608
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M. Zeiger,N. J?ckel,P. Strubel,L. Borchardt,R. Reinhold,W. Nickel,J. Eckert,V. Presser,S. Kaskel J. Mater. Chem. A, 2015,3, 17983-17990
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5. Distinct correlation between (CN2)x units and pores: a low-cost method for predesigned wide range control of micropore size of porous carbon?

Xiaotong Feng,Lei Bian,Jie Ma,Lei Zhou,Xiayan Wang,Guangsheng Guo,Qiaosheng Pu Chem. Commun., 2019,55, 3963-3966

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Additional information on 1-(2-Chloropyrimidin-4-yl)ethanol

Comprehensive Overview of 1-(2-Chloropyrimidin-4-yl)ethanol (CAS No. 1312535-79-7): Properties, Applications, and Industry Insights

1-(2-Chloropyrimidin-4-yl)ethanol (CAS No. 1312535-79-7) is a specialized heterocyclic compound that has garnered significant attention in pharmaceutical and agrochemical research. This compound, characterized by its pyrimidine backbone and chloro-substituted functional group, serves as a critical intermediate in the synthesis of bioactive molecules. Its unique structure enables versatile reactivity, making it a valuable building block for drug discovery and material science applications.

In recent years, the demand for high-purity intermediates like 1-(2-Chloropyrimidin-4-yl)ethanol has surged, driven by advancements in precision medicine and green chemistry. Researchers frequently search for "synthetic routes for chloropyrimidine derivatives" or "applications of pyrimidine-based alcohols," reflecting the compound's relevance in cutting-edge science. Its role in kinase inhibitor development and crop protection agents aligns with trending topics such as targeted cancer therapies and sustainable agriculture.

The physicochemical properties of 1312535-79-7 include a molecular weight of 174.59 g/mol and a distinct chloropyrimidine-ethanol hybrid structure, which facilitates selective bond formation in cross-coupling reactions. Analytical techniques like HPLC and NMR spectroscopy are commonly employed to verify its purity, a key concern for laboratories seeking "CAS 1312535-79-7 supplier specifications." The compound's stability under inert conditions makes it suitable for multistep organic synthesis.

From an industrial perspective, 1-(2-Chloropyrimidin-4-yl)ethanol exemplifies the growing market for custom chemical intermediates. Manufacturers emphasize scalable production methods to meet the needs of contract research organizations (CROs) and API developers. Environmental considerations have also prompted innovations in catalytic processes to reduce waste, addressing queries like "eco-friendly synthesis of pyrimidine alcohols." Regulatory compliance with REACH and GMP standards further underscores its commercial viability.

Emerging studies highlight the compound's potential in bioconjugation and proteomics, particularly for designing small-molecule probes. This aligns with the rise of "chemical biology tools" as a search trend among academic users. Additionally, its derivatization into chiral auxiliaries caters to the expanding field of asymmetric synthesis, a hot topic in organic chemistry forums.

In summary, 1-(2-Chloropyrimidin-4-yl)ethanol (CAS No. 1312535-79-7) represents a nexus of innovation across multiple disciplines. Its adaptability to structure-activity relationship (SAR) studies and compatibility with high-throughput screening platforms position it as a cornerstone for future breakthroughs. As industries prioritize molecular diversity and process efficiency, this compound will likely remain a focal point in both research and commercial applications.

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