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[1S-(1alpha,2beta,3alpha,5alpha)]-pinane-3-methylammonium chloride is a quaternary ammonium salt chemical compound characterized by a pinane ring structure and a methylammonium chloride group. The pinane ring is a bicyclic hydrocarbon with a cage-like shape, while the methylammonium chloride group is a salt derived from the reaction between methylamine and hydrochloric acid. [1S-(1alpha,2beta,3alpha,5alpha)]-pinane-3-methylammonium chloride's unique structural and chemical properties make it a versatile molecule with potential applications in organic synthesis, catalysis, and medicinal chemistry.

57357-84-3

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57357-84-3 Usage

Uses

Used in Organic Synthesis:
[1S-(1alpha,2beta,3alpha,5alpha)]-pinane-3-methylammonium chloride is used as a synthetic building block for the creation of various complex organic molecules. Its unique pinane ring structure and quaternary ammonium salt functionality allow for the development of novel chemical entities with potential applications in different industries.
Used in Catalysis:
In the field of catalysis, [1S-(1alpha,2beta,3alpha,5alpha)]-pinane-3-methylammonium chloride serves as a catalyst or a catalyst precursor. Its cationic nature and the presence of the pinane ring structure can facilitate specific chemical reactions, enhancing the efficiency and selectivity of the catalytic processes.
Used in Medicinal Applications:
[1S-(1alpha,2beta,3alpha,5alpha)]-pinane-3-methylammonium chloride is used as a potential therapeutic agent in the pharmaceutical industry. Its unique structure and chemical properties can be exploited to design new drugs targeting various diseases, including neurological disorders, cancer, and infectious diseases. [1S-(1alpha,2beta,3alpha,5alpha)]-pinane-3-methylammonium chloride's cationic nature may also allow it to interact with biological membranes and other cellular components, providing a basis for its medicinal applications.
Used in the Chemical Industry:
In the chemical industry, [1S-(1alpha,2beta,3alpha,5alpha)]-pinane-3-methylammonium chloride can be employed as an additive or a reagent in various chemical processes. Its cationic character and pinane ring structure may offer specific advantages in applications such as phase transfer catalysis, ion-exchange processes, or the synthesis of specialty chemicals.
Used in Material Science:
[1S-(1alpha,2beta,3alpha,5alpha)]-pinane-3-methylammonium chloride may also find applications in material science, where its unique structural and chemical properties can be utilized to develop new materials with tailored properties. These materials could have potential uses in areas such as sensors, energy storage, or advanced coatings.

Check Digit Verification of cas no

The CAS Registry Mumber 57357-84-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,3,5 and 7 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 57357-84:
(7*5)+(6*7)+(5*3)+(4*5)+(3*7)+(2*8)+(1*4)=153
153 % 10 = 3
So 57357-84-3 is a valid CAS Registry Number.

57357-84-3SDS

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,4S,5S)-N,4,6,6-tetramethylbicyclo[3.1.1]heptan-3-amine,hydrochloride

1.2 Other means of identification

Product number -
Other names -

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:57357-84-3 SDS

57357-84-3Relevant academic research and scientific papers

The TDE sulfenyl group as a protective group for amines

Netscher,Weller

, p. 8145 - 8154 (2007/10/02)

Various primary and secondary amines were transformed into their 2,2,2-trifluoro-1,1-diphenylethane- (TDE-) sulfenamides 5 in high yields. Efficient methods for cleavage and properties of these new derivatives are also described.

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