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16088-07-6

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16088-07-6 Usage

Uses

DL-Phenylalaninol may inhibit ulcer formation in rats, mainly by central inhibition of gastric acid secretion.

Check Digit Verification of cas no

The CAS Registry Mumber 16088-07-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,0,8 and 8 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 16088-07:
(7*1)+(6*6)+(5*0)+(4*8)+(3*8)+(2*0)+(1*7)=106
106 % 10 = 6
So 16088-07-6 is a valid CAS Registry Number.
InChI:InChI=1/C9H13NO/c10-9(7-11)6-8-4-2-1-3-5-8/h1-5,9,11H,6-7,10H2/p+1/t9-/m1/s1

16088-07-6 Well-known Company Product Price

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  • Alfa Aesar

  • (H63562)  DL-Phenylalaninol, 96%   

  • 16088-07-6

  • 1g

  • 365.0CNY

  • Detail
  • Alfa Aesar

  • (H63562)  DL-Phenylalaninol, 96%   

  • 16088-07-6

  • 5g

  • 1372.0CNY

  • Detail
  • Alfa Aesar

  • (H63562)  DL-Phenylalaninol, 96%   

  • 16088-07-6

  • 25g

  • 5468.0CNY

  • Detail

16088-07-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Amino-3-Phenyl-1-Propanol

1.2 Other means of identification

Product number -
Other names DL-Phenylalaninol

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:16088-07-6 SDS

16088-07-6Relevant articles and documents

Direct Access to Primary Amines from Alkenes by Selective Metal-Free Hydroamination

Du, Yi-Dan,Chen, Bi-Hong,Shu, Wei

supporting information, p. 9875 - 9880 (2021/03/29)

Direct and selective synthesis of primary amines from easily available precursors is attractive yet challenging. Herein, we report the rapid synthesis of primary amines from alkenes via metal-free regioselective hydroamination at room temperature. Ammonium carbonate was used as ammonia surrogate for the first time, allowing for efficient conversion of terminal and internal alkenes into linear, α-branched, and α-tertiary primary amines under mild conditions. This method provides a straightforward and powerful approach to a wide spectrum of advanced, highly functionalized primary amines which are of particular interest in pharmaceutical chemistry and other areas.

Regioselective Fluorination of α-Hydroxy-β-aminophosphonates by Using PyFluor

Ka?mierczak, Marcin,Kubicki, Maciej,Koroniak, Henryk

, p. 3844 - 3852 (2018/07/31)

We report a simple protocol for the synthesis of α-fluoro-β-aminophosphonates by the regioselective fluorination of α-hydroxy-β-aminophosphonates under mild conditions. The fluorination reactions were mediated by the PyFluor reagent and occurred with the retention of configuration. The main products of this reaction were a series of α-fluoro-β-aminophosphonates, which can be used as precursors in the preparation of medicinally important compounds (e.g., dipeptide analogues).

Probing o-diphenylphosphanyl benzoate (o-DPPB)-directed C - C bond formation: Total synthesis of dictyostatin

Wünsch, Sebastian,Breit, Bernhard

supporting information, p. 2358 - 2363 (2015/02/05)

Herein, we report a robust total synthesis of dictyostatin. This polyketide natural product has attracted much attention because of its impressive antiproliferative activity against several human cancer-cell lines. We accomplished its synthesis in a highly convergent manner from three fragments of equal complexity, which were prepared on multigram scale. The southern and northwestern subunits were constructed through application of our o-DPPB-directed hydroformylation and allylic substitution methodology, respectively. These methods generated the C6 and C14 stereocenters of dictyostatin with good diastereoselectivities and simultaneously allowed further elaboration of the fragments by Wittig olefination and Sharpless asymmetric epoxidation, respectively. The compelling performance of the hydroformylation and allylic substitution with regard to practicability, selectivity, and scale underline their value for the construction of propionate motifs.

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