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2-(Boc-AminoMethyl)pyrimidine is a chemical compound that belongs to the group known as Pyrimidines and pyrimidine derivatives. It features a pyrimidine ring, a six-membered heterocyclic ring structure composed of four carbon atoms, two nitrogen atoms, and their associated hydrogen atoms. The 'Boc' in its name stands for 'tert-butyl carbamate', a protecting group used in organic synthesis to prevent unwanted reactions in certain functional groups while other parts of the molecule undergo chemical reactions. 2-(Boc-aMinoMethyl)pyriMidine is found in industrial applications and is also utilized in laboratories for experimental purposes. Due to its chemical properties and potential hazards, it requires proper handling and storage.

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  • 1260843-26-2 Structure
  • Basic information

    1. Product Name: 2-(Boc-aMinoMethyl)pyriMidine
    2. Synonyms: 2-(Boc-aMinoMethyl)pyriMidine;2-(Boc-aMinoMethyl)pyriMi...;tert-butyl N-(pyrimidin-2-ylmethyl)carbamate
    3. CAS NO:1260843-26-2
    4. Molecular Formula: C10H15N3O2
    5. Molecular Weight: 209.245
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1260843-26-2.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: Sealed in dry,Room Temperature
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-(Boc-aMinoMethyl)pyriMidine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(Boc-aMinoMethyl)pyriMidine(1260843-26-2)
    11. EPA Substance Registry System: 2-(Boc-aMinoMethyl)pyriMidine(1260843-26-2)
  • Safety Data

    1. Hazard Codes: N/A
    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: 1260843-26-2(Hazardous Substances Data)

1260843-26-2 Usage

Uses

Used in Industrial Applications:
2-(Boc-AminoMethyl)pyrimidine is used as a chemical intermediate for the synthesis of various compounds in the chemical industry. Its Boc-protected aminomethyl group allows for controlled reactions, making it a valuable component in the production of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Laboratory Research:
In academic and research settings, 2-(Boc-AminoMethyl)pyrimidine is used as a reagent in the synthesis of complex organic molecules. Its Boc protection allows researchers to carry out selective reactions, facilitating the construction of intricate molecular structures and the exploration of new chemical pathways.
Used in Pharmaceutical Development:
2-(Boc-AminoMethyl)pyrimidine is used as a building block in the development of new drugs. Its presence in the molecular structure can influence the pharmacological properties of the final product, such as solubility, stability, and bioavailability. The Boc group can be selectively removed when needed, allowing for the introduction of other functional groups to enhance the drug's therapeutic effects.
Used in Agrochemical Production:
In the agrochemical industry, 2-(Boc-AminoMethyl)pyrimidine is used as a precursor in the synthesis of pesticides and other crop protection agents. Its Boc-protected structure enables the creation of molecules with specific biological activities, such as herbicidal, insecticidal, or fungicidal properties, which can be tailored to target specific pests or diseases.

Check Digit Verification of cas no

The CAS Registry Mumber 1260843-26-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,0,8,4 and 3 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1260843-26:
(9*1)+(8*2)+(7*6)+(6*0)+(5*8)+(4*4)+(3*3)+(2*2)+(1*6)=142
142 % 10 = 2
So 1260843-26-2 is a valid CAS Registry Number.

1260843-26-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl N-(pyrimidin-2-ylmethyl)carbamate

1.2 Other means of identification

Product number -
Other names tert-butyl (pyrimidin-2-ylmethyl)carbamate

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:1260843-26-2 SDS

1260843-26-2Relevant articles and documents

Synthesis method of 2-amino methyl pyrimidine hydrochloride and derivatives thereof

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Paragraph 0014; 0016; 0018; 0020; 0022, (2017/07/21)

The invention relates to preparation of one medicine intermediate, in particular relates to a preparation method of 2-aminomethylpyrimidine hydrochloride and derivatives thereof. The preparation method is improved by overcoming the defects of an industrial production technology and a laboratory technology which are commonly used at present, improvements are as follows: the method takes 2-cyanopyrimidine and derivatives thereof as starting materials, Boc anhydride is adopted as a protective agent, reduction-protection one-pot reaction is carried out under alkaline condition, and then hydrogen chloride deprotection is carried out, so that the 2-aminomethylpyrimidine hydrochloride and the derivatives thereof are prepared. According to the method provided by the invention, the reaction period is short, the conversion rate is high, the product quality is good, and the content of the produced 2-aminomethylpyrimidine hydrochloride and the derivatives thereof is more than 99%; meanwhile, operation steps are simple, required equipment is simple, and energy consumption is low.

COMPOUNDS AND RELATED COMPOSITIONS AND METHODS OF USE

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, (2013/03/26)

Compounds and compositions, which can be use for example, for treating cancer, are described herein.

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