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479064-93-2

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  • SAGECHEM/ (R)-3-((tert-Butoxycarbonyl)amino)-3-(4-chlorophenyl)propanoic acid /Manufacturer in China

    Cas No: 479064-93-2

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479064-93-2 Usage

General Description

Boc-(R)-3-Amino-3-(4-chlorophenyl)propionic acid is a chemical compound with the molecular formula C12H16ClNO4. It is a derivative of the amino acid phenylalanine, where the hydrogen atom on the alpha carbon is replaced with a tert-butoxycarbonyl (Boc) group. Boc-(R)-3-Amino-3-(4-chlorophenyl)propionic acid is a chiral molecule and exists as a pair of enantiomers, with the (R)-enantiomer being the one typically used in research and drug development. Boc-(R)-3-Amino-3-(4-chlorophenyl)propionic acid is primarily used as a building block for the synthesis of peptide-based compounds, such as peptidomimetics and pharmaceutical drugs. Its unique structural features make it a valuable tool in the field of medicinal chemistry and drug discovery.

Check Digit Verification of cas no

The CAS Registry Mumber 479064-93-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,9,0,6 and 4 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 479064-93:
(8*4)+(7*7)+(6*9)+(5*0)+(4*6)+(3*4)+(2*9)+(1*3)=192
192 % 10 = 2
So 479064-93-2 is a valid CAS Registry Number.
InChI:InChI=1/C14H18ClNO4/c1-14(2,3)20-13(19)16-11(8-12(17)18)9-4-6-10(15)7-5-9/h4-7,11H,8H2,1-3H3,(H,16,19)(H,17,18)/t11-/m1/s1

479064-93-2 Well-known Company Product Price

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  • Aldrich

  • (61902)  (R)-Boc-4-chloro-β-Phe-OH  ≥98.0% (HPLC)

  • 479064-93-2

  • 61902-500MG-F

  • 3,304.08CNY

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479064-93-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (3R)-3-(4-chlorophenyl)-3-[(2-methylpropan-2-yl)oxycarbonylamino]propanoic acid

1.2 Other means of identification

Product number -
Other names Boc-4-Chloro-D-b-phenylalanine

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:479064-93-2 SDS

479064-93-2Relevant articles and documents

α-Oxymethyl ketone enolates for the asymmetric Mannich reaction. From acetylene and N-alkoxycarbonylimines to β-amino acids

Palomo, Claudio,Oiarbide, Mikel,Gonzalez-Rego, M. Concepcion,Sharma, Arun K.,Garcia, Jesus M.,Gonzalez, Alberto,Landa, Cristina,Linden, Anthony

, p. 1063 - 1066 (2007/10/03)

The insufficient diastereoselectivity and generality, which are the main problems of the 'acetate' aza - aldol reaction, can now be addressed through the reaction of the lithium enolate of endo-O-trimethylsilyl acetyl isoborneol with various N[(p-tolylsul

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