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2-Azabicyclo[2.2.1]heptane, 2-methyl-, also known as 2-methyl-2-azabicyclo[2.2.1]heptane, is a bicyclic organic compound with a molecular formula of C8H15N and a molecular weight of 125.21 g/mol. It is a colorless liquid with a mild, amine-like odor and is insoluble in water but soluble in organic solvents. 2-Azabicyclo2.2.1heptane, 2-methylis commonly used as a building block in the synthesis of various pharmaceutical compounds and agrochemicals. Additionally, it has potential pharmacological properties and is being researched for its potential applications in drug discovery and development.

4524-95-2

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4524-95-2 Usage

Uses

Used in Pharmaceutical Industry:
2-Azabicyclo[2.2.1]heptane, 2-methylis used as a building block for the synthesis of various pharmaceutical compounds. Its unique bicyclic structure and amine-like properties make it a valuable component in the development of new drugs.
Used in Agrochemical Industry:
2-Azabicyclo[2.2.1]heptane, 2-methylis also used as a building block in the synthesis of agrochemicals. Its potential applications in this industry include the development of new pesticides, herbicides, and other agricultural chemicals.
Used in Drug Discovery and Development:
Due to its potential pharmacological properties, 2-Azabicyclo[2.2.1]heptane, 2-methylis being researched for its potential applications in drug discovery and development. Its unique structure and properties may contribute to the creation of novel therapeutic agents for various medical conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 4524-95-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,5,2 and 4 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4524-95:
(6*4)+(5*5)+(4*2)+(3*4)+(2*9)+(1*5)=92
92 % 10 = 2
So 4524-95-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H13N/c1-8-5-6-2-3-7(8)4-6/h6-7H,2-5H2,1H3

4524-95-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methyl-3-azabicyclo[2.2.1]heptane

1.2 Other means of identification

Product number -
Other names 2-methyl-2-azabicyclo<2.2.1>heptane

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:4524-95-2 SDS

4524-95-2Synthetic route

2-methyl-2-azabicyclo<2.2.1>hept-5-ene
95019-15-1

2-methyl-2-azabicyclo<2.2.1>hept-5-ene

2-methyl-2-azabicyclo<2.2.1>heptane
4524-95-2

2-methyl-2-azabicyclo<2.2.1>heptane

Conditions
ConditionsYield
With hydrogen; palladium on activated charcoal In diethyl ether for 6h;90%
cyclopenta-1,3-diene
542-92-7

cyclopenta-1,3-diene

2-methyl-2-azabicyclo<2.2.1>heptane
4524-95-2

2-methyl-2-azabicyclo<2.2.1>heptane

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: 80 percent / H2O / 4 h / Ambient temperature
2: 90 percent / H2 / Pd/C / diethyl ether / 6 h
View Scheme

4524-95-2Downstream Products

4524-95-2Relevant academic research and scientific papers

NMR Studies of N-Methyl Derivatives of the 2-Azabicycloheptyl and -octyl Ring System; Kinetic Protonation in Determination of Invertomer Preferences

Belkacemi, Djaballah,Malpass, John R.

, p. 9105 - 9116 (2007/10/02)

The title compounds were studied by 1H, 13C, and 15N NMR spectroscopy.Since inversion at nitrogen is rapid on the NMR time scale even at low temperatures, kinetic protonation was used to estimate invertomer ratios at ambient temperature.Invertomer preferences appear to be consistent with the operation of steric factors.

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