Phenibut (β-Phenyl-GABA HCl)

Basic information

  • Product Name:Phenibut (β-Phenyl-GABA HCl)
  • CasNo.:3060-41-1
  • MF:C10H14ClNO2
  • MW:215.68

Physical and Chemical Properties

  • Purity:99%
  • Boiling Point:194-201 °C
  • Packing:White crystalline powder
  • Throughput:
Inquiry

Product Details

CasNo: 3060-41-1

MF: C10H14ClNO2

Appearance: White crystalline powder

Factory Export Top Purity Phenibut (β-Phenyl-GABA HCl) 3060-41-1 In Stock

  • Molecular Formula:C10H14ClNO2
  • Molecular Weight:215.68
  • Appearance/Colour:White crystalline powder 
  • Vapor Pressure:7.09E-05mmHg at 25°C 
  • Melting Point:194-201 °C 
  • Boiling Point:327.8 °C at 760 mmHg 
  • Flash Point:152.1 °C 
  • PSA:63.32000 
  • Density:1.161g/cm3 
  • LogP:2.53340 

3-Amino-4-phenylbutyric acid hydrochloride(Cas 3060-41-1) Usage

InChI:InChI=1/C10H13NO2.ClH/c11-9(7-10(12)13)6-8-4-2-1-3-5-8;/h1-5,9H,6-7,11H2,(H,12,13);1H

3060-41-1 Relevant articles

Divergent Synthesis of γ-Amino Acid and γ-Lactam Derivatives from meso-Glutaric Anhydrides

Connon, Stephen J.,Craig, Ryan,Smith, Simon N.

supporting information, p. 13378 - 13382 (2020/10/02)

The first divergent synthesis of both γ-...

Preparation method for synthesizing 4-amino-3-phenylbutyric acid hydrochloride by one-pot method and product prepared by preparation method

-

Paragraph 0031-0060, (2020/07/21)

The invention discloses a preparation me...

Assembling of medium/long chain-based β-arylated unnatural amino acid derivatives via the Pd(II)-catalyzed sp3 β-C-H arylation and a short route for rolipram-type derivatives

Tomar, Radha,Bhattacharya, Debabrata,Babu, Srinivasarao Arulananda

, p. 2447 - 2465 (2019/03/26)

In this paper, we report the assembling ...

A novel method for the synthesis of racemic pregabalin, baclofen and 3-phenibut involving lossen rearrangement

Ponnusamy, Kannan,Davis Presley,Nagapillai, Prakash,Deivanayagam, Eswaramoorthy

, p. 275 - 278 (2018/09/14)

Pregabalin,baclofen,and3-phenibutareγ-am...

3060-41-1 Process route

4-phenylpyrrolidin-2-one
1198-97-6

4-phenylpyrrolidin-2-one

(±)-3-carboxy-2-phenylpropan-1-aminium chloride
3060-41-1,52950-37-5

(±)-3-carboxy-2-phenylpropan-1-aminium chloride

Conditions
Conditions Yield
With hydrogenchloride; water; for 12h; Reflux;
88%
With hydrogenchloride; In water; for 12h; Reflux;
88%
With hydrogenchloride; In water; for 16h; Sealed tube; Reflux;
65%
With hydrogenchloride; water; In water; for 16h; Reflux;
55%
α-phenyl-β-benzoyl-γ-nitrobutyrate ethyl ester
62384-61-6

α-phenyl-β-benzoyl-γ-nitrobutyrate ethyl ester

(±)-3-carboxy-2-phenylpropan-1-aminium chloride
3060-41-1,52950-37-5

(±)-3-carboxy-2-phenylpropan-1-aminium chloride

Conditions
Conditions Yield
α-phenyl-β-benzoyl-γ-nitrobutyrate ethyl ester; With hydrogen; In methanol; at 38 - 42 ℃; for 7h; under 11251.1 - 30003 Torr;
With hydrogenchloride; In water; at 90 - 100 ℃; for 1h; Reagent/catalyst;

3060-41-1 Upstream products

  • 71639-13-9
    71639-13-9

    diethyl 2-(3-nitrophenylethyl)malonate

  • 1198-97-6
    1198-97-6

    4-phenylpyrrolidin-2-one

  • 98-80-6
    98-80-6

    phenylboronic acid

  • 41441-40-1
    41441-40-1

    ethyl 3-phenyl-4-nitrobutanoate

3060-41-1 Downstream products

  • 106869-48-1
    106869-48-1

    4-phenyl-1-(trimethylsilyl)-2-pyrrolidinone

  • 189014-01-5
    189014-01-5

    4-((tert-butoxycarbonyl)amino)-3-phenylbutanoic acid

  • 189014-03-7
    189014-03-7

    (3-Hydroxycarbamoyl-2-phenyl-propyl)-carbamic acid tert-butyl ester

  • 189014-02-6
    189014-02-6

    4-tert-Butoxycarbonylamino-3-phenyl-butyric acid 2,5-dioxo-pyrrolidin-1-yl ester