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N-BENZOYL-DL-THREONINE is a chemical compound derived from the amino acid threonine, featuring a benzoyl group that serves as a chiral precursor in the synthesis of pharmaceuticals and biologically active compounds. Its unique structure enables the production of enantiopure compounds, making it a valuable asset in the pharmaceutical industry and medicinal chemistry.

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  • 7469-23-0 Structure
  • Basic information

    1. Product Name: N-BENZOYL-DL-THREONINE
    2. Synonyms: (±)-N-Benzoylthreonine;Nsc401323;N-BENZOYL-DL-THREONINE;Bz-DL-Thr-OH;N-Benzoyl-DL-threonine,tech.85%
    3. CAS NO:7469-23-0
    4. Molecular Formula: C11H13NO4
    5. Molecular Weight: 223.23
    6. EINECS: 231-264-7
    7. Product Categories: N/A
    8. Mol File: 7469-23-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: 1.573
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: N-BENZOYL-DL-THREONINE(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-BENZOYL-DL-THREONINE(7469-23-0)
    11. EPA Substance Registry System: N-BENZOYL-DL-THREONINE(7469-23-0)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: S22:Do not inhale dust.; S24/25:Avoid contact with skin and eyes.;
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 7469-23-0(Hazardous Substances Data)

7469-23-0 Usage

Uses

Used in Pharmaceutical Industry:
N-BENZOYL-DL-THREONINE is used as a chiral precursor for the synthesis of various medications and synthetic organic compounds. Its benzoyl group allows for the production of enantiopure compounds, which is crucial for the development of effective and safe pharmaceuticals.
Used in Medicinal Chemistry and Drug Discovery:
N-BENZOYL-DL-THREONINE is utilized as a key compound in the development of new drugs and biologically active molecules. Its ability to act as a chiral source contributes to the advancement of innovative therapeutic agents and the discovery of novel pharmaceutical compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 7469-23-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,6 and 9 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 7469-23:
(6*7)+(5*4)+(4*6)+(3*9)+(2*2)+(1*3)=120
120 % 10 = 0
So 7469-23-0 is a valid CAS Registry Number.
InChI:InChI=1/C11H13NO4/c1-7(13)9(11(15)16)12-10(14)8-5-3-2-4-6-8/h2-7,9,13H,1H3,(H,12,14)(H,15,16)/t7?,9-/m0/s1

7469-23-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N-BENZOYL-DL-THREONINE

1.2 Other means of identification

Product number -
Other names N-Benzoyl-DL-threonine,tech.

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:7469-23-0 SDS

7469-23-0Relevant articles and documents

Reactivity of α-Amino Acids in the Reaction with Esters in Aqueous–1,4-Dioxane Media

Kochetova,Kustova,Kuritsyn

, p. 80 - 85 (2018/03/09)

The kinetics of the reaction of a series of α-amino acids with 4-nitrophenyl acetate, 4-nitrophenyl benzoate, and 2,4,6-trinitrophenyl benzoate in aqueous 1,4-dioxane medium has been studied. Kinetics of the reactions involving 4-nitrophenyl acetate and 2,4,6-trinitrophenyl benzoate has complied with the Br?nsted dependence and revealed linear correlation between rate constant logarithm and the energy difference of the frontier orbitals of α-amino acids anions.

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