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(R)-2-AMINO-3-METHYL-1 1-DIPHENYLBUTANE is a chiral compound characterized by a 1,1-diphenylbutane backbone, with a methyl group and an amino group attached to the second carbon atom. This unique structure endows it with significant applications in various fields due to its chiral nature, which is crucial for creating enantioselective compounds and studying asymmetric reactions in organic chemistry.

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  • 400870-29-3 Structure
  • Basic information

    1. Product Name: (R)-2-AMINO-3-METHYL-1 1-DIPHENYLBUTANE&
    2. Synonyms: Benzeneethanamine, α-(1-methylethyl)-β-phenyl-, (αR)-
    3. CAS NO:400870-29-3
    4. Molecular Formula: C17H21N
    5. Molecular Weight: 239.36
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 400870-29-3.mol
  • Chemical Properties

    1. Melting Point: 73-76 °C(lit.)
    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: (R)-2-AMINO-3-METHYL-1 1-DIPHENYLBUTANE&(CAS DataBase Reference)
    10. NIST Chemistry Reference: (R)-2-AMINO-3-METHYL-1 1-DIPHENYLBUTANE&(400870-29-3)
    11. EPA Substance Registry System: (R)-2-AMINO-3-METHYL-1 1-DIPHENYLBUTANE&(400870-29-3)
  • Safety Data

    1. Hazard Codes: Xi
    2. Statements: 36/37/38
    3. Safety Statements: 26-36
    4. WGK Germany: 3
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 400870-29-3(Hazardous Substances Data)

400870-29-3 Usage

Uses

Used in Pharmaceutical Synthesis:
(R)-2-AMINO-3-METHYL-1 1-DIPHENYLBUTANE is utilized as a chiral building block in the synthesis of various pharmaceuticals and biologically active molecules. Its presence in the molecular structure can influence the drug's efficacy, selectivity, and potential side effects, making it a valuable component in drug development.
Used in Asymmetric Catalysis:
In the field of catalysis, (R)-2-AMINO-3-METHYL-1 1-DIPHENYLBUTANE serves as a ligand, playing a vital role in asymmetric catalysis. This application is essential for producing enantiomerically pure compounds, which are crucial in the pharmaceutical industry, as the different enantiomers of a drug can have significantly different biological activities.
Used in Chiral Auxiliary Preparation:
(R)-2-AMINO-3-METHYL-1 1-DIPHENYLBUTANE is also employed in the preparation of chiral auxiliaries for asymmetric synthesis. These auxiliaries are temporary components added to a molecule during a chemical reaction to control its stereochemistry, ensuring the production of the desired enantiomer with high selectivity.
Used in Organic Chemistry Research:
The chiral nature of (R)-2-AMINO-3-METHYL-1 1-DIPHENYLBUTANE makes it an important tool for studying asymmetric reactions in organic chemistry. Understanding these reactions is crucial for developing new synthetic methods and designing more efficient and selective chemical processes.

Check Digit Verification of cas no

The CAS Registry Mumber 400870-29-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,0,8,7 and 0 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 400870-29:
(8*4)+(7*0)+(6*0)+(5*8)+(4*7)+(3*0)+(2*2)+(1*9)=113
113 % 10 = 3
So 400870-29-3 is a valid CAS Registry Number.

400870-29-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (2R)-3-methyl-1,1-diphenylbutan-2-amine

1.2 Other means of identification

Product number -
Other names (R)-(+)-2-Amino-3-methyl-1,1-diphenylbutane

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:400870-29-3 SDS

400870-29-3Downstream Products

400870-29-3Relevant articles and documents

COMPOSITIONS AND METHODS FOR CYCLOFRUCTANS AS SEPARATION AGENTS

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Page/Page column 45-49; 61, (2010/12/31)

The present invention relates to derivatized cyclofructan compounds, compositions comprising derivatized cyclofructan compounds, and methods of using compositions comprising derivatized cyclofructan compounds for chromatographic separations of chemical species, including enantiomers. Said compositions may comprise a solid support and/or polymers comprising derivatized cyclofructan compounds.

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