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(S)-2-Amino-3-methyl-1,1-diphenyl-1-butanol is a complex organic compound that belongs to the group of amino alcohols. It is characterized by the presence of an amino group (-NH2), two phenyl ring structures, a secondary alcohol group (-OH), and a methyl group (-CH3). The "(S)-" prefix in its name indicates that it has a specific configuration in chiral (asymmetric) carbon atoms, following the Cahn-Ingold-Prelog priority rules, which means it only rotates the plane-polarized light in one direction. Amino alcohols like this compound are often utilized in the synthesis of pharmaceuticals and as intermediates in organic synthesis.

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  • 130432-39-2 Structure
  • Basic information

    1. Product Name: (S)- 2-Amino-3-methyl-1,1-diphenyl-1-butanol
    2. Synonyms: (S)-(-)-2-Amino-3-methyl-1,1-diphenyl-1-butanol hydrochloride;S-2-amino-3-methyl-1,1-diphenylbutan-1-ol;(2S)-2-amino-3-methyl-1,1-diphenylbutan-1-ol,hydrochloride
    3. CAS NO:130432-39-2
    4. Molecular Formula: C17H21NO.ClH
    5. Molecular Weight: 291.82
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 130432-39-2.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 451.4 °C at 760 mmHg
    3. Flash Point: 226.8 °C
    4. Appearance: /
    5. Density: N/A
    6. Vapor Pressure: 6.16E-09mmHg at 25°C
    7. Refractive Index: N/A
    8. Storage Temp.: Sealed in dry,Room Temperature
    9. Solubility: N/A
    10. CAS DataBase Reference: (S)- 2-Amino-3-methyl-1,1-diphenyl-1-butanol(CAS DataBase Reference)
    11. NIST Chemistry Reference: (S)- 2-Amino-3-methyl-1,1-diphenyl-1-butanol(130432-39-2)
    12. EPA Substance Registry System: (S)- 2-Amino-3-methyl-1,1-diphenyl-1-butanol(130432-39-2)
  • 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: 130432-39-2(Hazardous Substances Data)

130432-39-2 Usage

Uses

Used in Pharmaceutical Synthesis:
(S)-2-Amino-3-methyl-1,1-diphenyl-1-butanol is used as a key intermediate in the synthesis of various pharmaceuticals. Its unique structure allows it to be a versatile building block for creating complex molecules with potential therapeutic applications.
Used in Organic Synthesis:
In the field of organic synthesis, (S)-2-Amino-3-methyl-1,1-diphenyl-1-butanol is employed as an intermediate for the preparation of a wide range of organic compounds. Its functional groups, such as the amino and alcohol groups, can be further modified to produce a variety of derivatives with different properties and applications.

Check Digit Verification of cas no

The CAS Registry Mumber 130432-39-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,4,3 and 2 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 130432-39:
(8*1)+(7*3)+(6*0)+(5*4)+(4*3)+(3*2)+(2*3)+(1*9)=82
82 % 10 = 2
So 130432-39-2 is a valid CAS Registry Number.
InChI:InChI=1/C17H21NO.ClH/c1-13(2)16(18)17(19,14-9-5-3-6-10-14)15-11-7-4-8-12-15;/h3-13,16,19H,18H2,1-2H3;1H/t16-;/m0./s1

130432-39-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S)-2-amino-3-methyl-1,1-diphenylbutan-1-ol,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:130432-39-2 SDS

130432-39-2Downstream Products

130432-39-2Relevant articles and documents

Ethynylbenziodoxolones (EBX) as reagents for the ethynylation of stabilized enolates

Fernandez Gonzalez, Davinia,Brand, Jonathan P.,Mondiere, Regis,Waser, Jerome

supporting information, p. 1631 - 1639 (2013/07/05)

Herein, we report a detailed study on the electrophilic alkynylation of cyclic keto esters and amides with ethynylbenziodoxolone (EBX) reagents. The structure and stability of this class of reagents is first described more in details. Differential scannin

Straightforward synthesis of chiral hydroxy isocyanides

Bauer, Michael,Kazmaier, Uli

experimental part, p. 2360 - 2366 (2009/09/05)

Various types of hydroxy isocyanides have been prepared from the corresponding amino alcohols. These hydroxy isocyanides are interesting building blocks for multicomponent reactions and the synthesis of (hydroxyalkyl) oxazoline ligands. The isocyanides ar

Synthesis of chiral tetraaminophosphonium chlorides from N-Boc α-amino acid esters

Uraguchi, Daisuke,Sakaki, Sawako,Ueki, Yusuke,Ito, Takaki,Ooi, Takashi

scheme or table, p. 1081 - 1085 (2009/06/28)

Preparation of chiral tetraaminophosphonium chlorides of type 1 starting from N-Boc α-amino acid esters is described. Modified conditions for the displacement of the tertiary hydroxy group of the intermediary amino alcohol pave a way for the assembly of 1

Orally Bioavailable Caffeic Acid Related Anticancer Drugs

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Page/Page column 18, (2008/06/13)

The present invention concerns compounds and their use to treat cell proliferative diseases such as cancer. Compounds of the present invention display significant potency as inhibitors of Jak2/STAT3 pathways and downstream targets and inhibit the growth and survival of cancerous cell lines.

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