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14464-67-6

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14464-67-6 Usage

Chemical Properties

White powder

Check Digit Verification of cas no

The CAS Registry Mumber 14464-67-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,4,6 and 4 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 14464-67:
(7*1)+(6*4)+(5*4)+(4*6)+(3*4)+(2*6)+(1*7)=106
106 % 10 = 6
So 14464-67-6 is a valid CAS Registry Number.
InChI:InChI=1/C10H10F3NO2/c11-10(12,13)7-3-1-2-6(4-7)5-8(14)9(15)16/h1-4,8H,5,14H2,(H,15,16)/t8-/m1/s1

14464-67-6 Well-known Company Product Price

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  • Alfa Aesar

  • (H27508)  3-(Trifluoromethyl)-D-phenylalanine, 97%   

  • 14464-67-6

  • 250mg

  • 880.0CNY

  • Detail
  • Alfa Aesar

  • (H27508)  3-(Trifluoromethyl)-D-phenylalanine, 97%   

  • 14464-67-6

  • 1g

  • 2264.0CNY

  • Detail

14464-67-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(Trifluoromethyl)-D-phenylalanine

1.2 Other means of identification

Product number -
Other names (R)-2-Amino-3-(3-(trifluoromethyl)phenyl)propanoic acid

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:14464-67-6 SDS

14464-67-6Relevant articles and documents

Asymmetric synthesis, biological activity and molecular docking studies of some unsaturated α-amino acids, derivatives of glycine, allylglycine and propargylglycine

Hayriyan, Liana A.,Karapetyan, Ani J.,Minasyan, Ella V.,Mkrtchyan, Anna F.,Paloyan, Ani M.,Panosyan, Henrik A.,Poghosyan, Artavazd S.,Saghyan, Ashot S.,Sahakyan, Lusine Yu.,Sargsyan, Armen S.,Tovmasyan, Anna S.,Tsaturyan, Avetis H.

, (2020/02/18)

New enantiomerically enriched unsaturated tailor-made amino acids have been obtained. As a starting amino acid synthon for the asymmetric synthesis of tailor-made unsaturated amino acids, Ni(II) square-planar complexes of Schiff's bases of propargylglycine, allylglycine and glycine with chiral auxiliary (S)-2-N-(N’-benzylprolyl)-aminobenzophenone ((S)-BPB) were used. The Cα-alkylation of propargylglycine, allylglycine and glycine moieties resulted in the asymmetric synthesis of novel (S)-α-propargylglycine, (S)-α-allylglycine and glycine derivatives containing an aromatic group in the side chain (de 80–95,5%). After purification and cleavage of the metal complexes, the amino acids were isolated in high enantiomeric purity (ee >99%). Of the obtained seven tailor-made amino acids four showed inhibitory activity to collagenase G. The amino acid with an acetylene bond in the side chain (IC50 = 1.29 ± 0.02 mM) had the best result. Molecular docking showed that the amino acids with activity to collagenase G contained hydrogen and π-π bonds with the enzyme.

Preparation of (R)-Phenylalanine Analogues by Enantioselective Destruction Using L-Amino Acid Oxidase

Pirrung, Michael C.,Krishnamurthy, N.

, p. 957 - 958 (2007/10/02)

-

Synthesis and antifertility activity of 4- and 5-(omega-arylalkyl) oxazolidinethiones.

Lednicer,Emmert

, p. 1258 - 1262 (2007/10/05)

-

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