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3-(BOC-AMINO)-3-METHYLAZETIDINE is a chemical compound characterized by its molecular formula C10H19NO3. It is a derivative of azetidine, featuring a four-membered nitrogen-containing ring. The "3-(BOC-AMINO)" component indicates the presence of a BOC-protected amine group, which is a common feature in organic synthesis. 3-(BOC-AMINO)-3-METHYLAZETIDINE is known for its role as a building block in the creation of pharmaceuticals and agrochemicals, and also serves as a reagent in organic chemistry due to its distinctive structural attributes.

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  • 1018443-01-0 Structure
  • Basic information

    1. Product Name: 3-(BOC-AMINO)-3-METHYLAZETIDINE
    2. Synonyms: 3-(BOC-AMINO)-3-METHYLAZETIDINE;3-(Boc-aMino)-3-Methylaze...;tert-Butyl (3-methylazetidin-3-yl)carbamate;(3-Methyl-azetidin-3-yl)-carbamic acid tert-butyl ester
    3. CAS NO:1018443-01-0
    4. Molecular Formula: C9H18N2O2
    5. Molecular Weight: 186.25142
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1018443-01-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 270.6±29.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.04±0.1 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: 2-8°C
    8. Solubility: N/A
    9. PKA: 10.26±0.20(Predicted)
    10. CAS DataBase Reference: 3-(BOC-AMINO)-3-METHYLAZETIDINE(CAS DataBase Reference)
    11. NIST Chemistry Reference: 3-(BOC-AMINO)-3-METHYLAZETIDINE(1018443-01-0)
    12. EPA Substance Registry System: 3-(BOC-AMINO)-3-METHYLAZETIDINE(1018443-01-0)
  • 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: 1018443-01-0(Hazardous Substances Data)

1018443-01-0 Usage

Uses

Used in Pharmaceutical Synthesis:
3-(BOC-AMINO)-3-METHYLAZETIDINE is used as a building block for the synthesis of various pharmaceuticals. Its unique structure and BOC-protected amine group contribute to the development of new drugs with potential therapeutic applications.
Used in Agrochemical Production:
In the agrochemical industry, 3-(BOC-AMINO)-3-METHYLAZETIDINE is utilized as a key component in the synthesis of compounds designed to protect crops and enhance agricultural productivity. Its structural features make it a valuable asset in creating effective and targeted agrochemicals.
Used as a Reagent in Organic Chemistry:
3-(BOC-AMINO)-3-METHYLAZETIDINE also serves as a reagent in organic chemistry reactions. Its distinctive structural elements allow it to participate in a variety of chemical processes, facilitating the synthesis of complex organic molecules for research and industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 1018443-01-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,1,8,4,4 and 3 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1018443-01:
(9*1)+(8*0)+(7*1)+(6*8)+(5*4)+(4*4)+(3*3)+(2*0)+(1*1)=110
110 % 10 = 0
So 1018443-01-0 is a valid CAS Registry Number.

1018443-01-0SDS

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 tert-butyl N-(3-methylazetidin-3-yl)carbamate

1.2 Other means of identification

Product number -
Other names 3-(Boc-Amino)-3-methylazetidine

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:1018443-01-0 SDS

1018443-01-0Downstream Products

1018443-01-0Relevant articles and documents

Melanin Concentrating Hormone Receptor-1 Antagonist Pyridinones

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Page/Page column 72-73, (2010/11/30)

The present invention provides for MCHR1 antagonist compounds of formula (I) and the pharmaceutically acceptable salts, solvates and prodrugs thereof, wherein the substituents are as defined herein, and the pharmaceutically acceptable salts, solvates and

ANTAGONISTS OF SNS SODIUM CHANNELS

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Page/Page column 36, (2010/11/25)

Compounds of the formula (I), and pharmaceutically acceptable salts thereof, are found to be antagonists of SNS sodium channels. They are therefore useful as analgesic and neuroprotective agents, formula (I): R1 represents: (a) -L-A or -L' -A'

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