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[1R,4S,(+)]-N,2,3,3-Tetramethylbicyclo[2.2.1]heptane-2-amine, commonly known as menthylamine, is a bicyclic compound featuring a tertiary amine group. It is recognized for its rigid structure and ability to influence the stereochemistry of chemical reactions, making it a valuable asset in various scientific and industrial applications.

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  • 107538-05-6 Structure
  • Basic information

    1. Product Name: [1R,4S,(+)]-N,2,3,3-Tetramethylbicyclo[2.2.1]heptane-2-amine
    2. Synonyms: [1R,4S,(+)]-N,2,3,3-Tetramethylbicyclo[2.2.1]heptane-2-amine;Dexmecamylamine
    3. CAS NO:107538-05-6
    4. Molecular Formula: C11H21N
    5. Molecular Weight: 167.29
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 107538-05-6.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.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: [1R,4S,(+)]-N,2,3,3-Tetramethylbicyclo[2.2.1]heptane-2-amine(CAS DataBase Reference)
    10. NIST Chemistry Reference: [1R,4S,(+)]-N,2,3,3-Tetramethylbicyclo[2.2.1]heptane-2-amine(107538-05-6)
    11. EPA Substance Registry System: [1R,4S,(+)]-N,2,3,3-Tetramethylbicyclo[2.2.1]heptane-2-amine(107538-05-6)
  • 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: 107538-05-6(Hazardous Substances Data)

107538-05-6 Usage

Uses

Used in Organic Synthesis:
Menthylamine is utilized as a chiral auxiliary in organic synthesis, where its rigid structure aids in controlling the stereochemistry of reactions. This application is crucial for the production of pharmaceuticals and agrochemicals, ensuring the desired stereoisomer is obtained.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, [1R,4S,(+)]-N,2,3,3-Tetramethylbicyclo[2.2.1]heptane-2-amine is used as a key component in the synthesis of various drugs. Its role in controlling stereochemistry is vital for the development of effective and safe medications.
Used in Agrochemical Industry:
Similarly, in the agrochemical industry, menthylamine is employed in the synthesis of pesticides and other chemical products, where stereochemistry plays a significant role in their efficacy and safety.
Used in Flavor and Fragrance Industry:
Menthylamine also finds application in the flavor and fragrance industry, where it imparts a minty and cooling sensation to products, enhancing the sensory experience for consumers.

Check Digit Verification of cas no

The CAS Registry Mumber 107538-05-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,5,3 and 8 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 107538-05:
(8*1)+(7*0)+(6*7)+(5*5)+(4*3)+(3*8)+(2*0)+(1*5)=116
116 % 10 = 6
So 107538-05-6 is a valid CAS Registry Number.
InChI:InChI=1/C11H21N/c1-10(2)8-5-6-9(7-8)11(10,3)12-4/h8-9,12H,5-7H2,1-4H3/t8-,9+,11+/m1/s1

107538-05-6SDS

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 (1S,3S,4R)-N,2,2,3-tetramethylbicyclo[2.2.1]heptan-3-amine

1.2 Other means of identification

Product number -
Other names mecamylamine

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:107538-05-6 SDS

107538-05-6Upstream product

107538-05-6Downstream Products

107538-05-6Relevant articles and documents

Alkylated bicycloalkaneamines for treatment of neurotoxic injury

-

, (2008/06/13)

Compounds, compositions and methods of treatment are described to control brain damage associated with anoxia or ischemia which typically follows such conditions as stroke, cardiac arrest or perinatal asphyxia. The treatment includes administration of an alkylated bicycloalkaneamine compound as an antagonist to inhibit excitotoxic actions at major neuronal exzcitatory amino acid receptor sites.

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