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84863-67-2

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84863-67-2 Usage

Description

[(1S)-3-methyl-1-[[(3-methylbutyl)amino] is a complex organic molecule belonging to the amine class, characterized by the presence of a nitrogen atom bonded to three hydrogen atoms. It consists of a 3-methyl-1 molecule, which contains a methyl group, a common structural unit in organic chemistry, and a butylamino group, which features a four-carbon chain bonded to an amino group. The unique combination of these structural elements endows [(1S)-3-methyl-1-[[(3-methylbutyl)amino] with distinct chemical properties, making it suitable for various applications in different industries.

Uses

Used in Pharmaceutical Industry:
[(1S)-3-methyl-1-[[(3-methylbutyl)amino] is used as an active pharmaceutical ingredient for [application reason], such as targeting specific biological pathways or receptors, due to its unique chemical structure and properties.
Used in Chemical Synthesis:
In the chemical synthesis industry, [(1S)-3-methyl-1-[[(3-methylbutyl)amino] is used as a building block or intermediate for the synthesis of more complex molecules, taking advantage of its reactive functional groups and structural features.
Used in Research and Development:
[(1S)-3-methyl-1-[[(3-methylbutyl)amino] is utilized in research and development as a model compound to study the effects of structural modifications on the properties and reactivity of amine-based molecules, contributing to the advancement of organic chemistry and related fields.
Used in Material Science:
In the material science field, [(1S)-3-methyl-1-[[(3-methylbutyl)amino] is used as a component in the development of novel materials with specific properties, such as improved conductivity, stability, or reactivity, based on its unique molecular structure and chemical characteristics.

Check Digit Verification of cas no

The CAS Registry Mumber 84863-67-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,8,6 and 3 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 84863-67:
(7*8)+(6*4)+(5*8)+(4*6)+(3*3)+(2*6)+(1*7)=172
172 % 10 = 2
So 84863-67-2 is a valid CAS Registry Number.

84863-67-2SDS

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 (S)-2-(tert-butoxycarbonylamino)-N-isopentyl-4-methylpentanamide

1.2 Other means of identification

Product number -
Other names N-(Boc-L-leucyl)isopentylamine

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:84863-67-2 SDS

84863-67-2Relevant articles and documents

COMPOSITIONS AND METHODS FOR SYNTHESIZING (2S,3S)-TRANS-EPOXYSUCCINYL-L-LEUCYL-AMIDO-3-METHYLBUTANE ETHYL ESTER

-

Paragraph 0056; 0059; 0066; 0067; 0110; 0111, (2017/07/06)

In alternative embodiments the invention provides methods for synthesizing AB-007 (also called loxistatin, E64d, EST or ((2S,3S)-trans-epoxysuccinyl-L-leucyl-amido-3-methylbutane ethyl ester) and its acid form E64c (loxistatin acid), and various synthetic

Influence of neighboring groups on the thermodynamics of hydrophobic binding: An added complex facet to the hydrophobic effect

Nasief, Nader N.,Hangauer, David

supporting information, p. 2315 - 2333 (2014/04/17)

The thermodynamic consequences of systematic modifications in a ligand side chain that binds in a shallow hydrophobic pocket, in the presence and absence of a neighboring ligand carboxylate group, were evaluated using isothermal titration calorimetry (ITC

Design, synthesis and evaluation of 3-methylene-substituted indolinones as antimalarials

Praveen Kumar,Gut, Jiri,Guedes, Rita C.,Rosenthal, Philip J.,Santos, Maria M.M.,Moreira, Rui

experimental part, p. 927 - 933 (2011/04/16)

The design, synthesis and evaluation of 3-methylene-substituted indolinones as falcipain inhibitors and antiplasmodial agents are described. These compounds react readily with thiols via an addition-elimination mechanism, indicating their potential as cys

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