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N-CBZ-DL-TRYPTOPHAN is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 13058-16-7 Structure
  • Basic information

    1. Product Name: N-CBZ-DL-TRYPTOPHAN
    2. Synonyms: N-ALPHA-CARBOBENZOXY-DL-TRYPTOPHAN;N-CARBOBENZOXY-DL-TRYPTOPHAN;N-CBZ-DL-TRYPTOPHAN;N-BENZYLOXYCARBONYL-DL-TRYPTOPHAN;Z-DL-TRP;Z-DL-TRP-OH;Z-DL-TRYPTOPHAN;AKOS BBS-00007675
    3. CAS NO:13058-16-7
    4. Molecular Formula: C19H18N2O4
    5. Molecular Weight: 338.36
    6. EINECS: 235-949-1
    7. Product Categories: Amino Acids;Amino Acids (N-Protected);Biochemistry;Cbz-Amino Acids;Indoles;Tryptophans;Amino Acids;I - Z;Modified Amino Acids
    8. Mol File: 13058-16-7.mol
  • Chemical Properties

    1. Melting Point: 170 °C
    2. Boiling Point: 619.1°Cat760mmHg
    3. Flash Point: 328.2°C
    4. Appearance: /
    5. Density: 1.341g/cm3
    6. Vapor Pressure: 3.46E-16mmHg at 25°C
    7. Refractive Index: 1.662
    8. Storage Temp.: 2-8°C
    9. Solubility: almost transparency in Methanol
    10. PKA: 3.98±0.10(Predicted)
    11. CAS DataBase Reference: N-CBZ-DL-TRYPTOPHAN(CAS DataBase Reference)
    12. NIST Chemistry Reference: N-CBZ-DL-TRYPTOPHAN(13058-16-7)
    13. EPA Substance Registry System: N-CBZ-DL-TRYPTOPHAN(13058-16-7)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: 24/25
    4. WGK Germany: 3
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 13058-16-7(Hazardous Substances Data)

13058-16-7 Usage

Chemical Properties

Light yellow crystals or powder

Check Digit Verification of cas no

The CAS Registry Mumber 13058-16-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,0,5 and 8 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 13058-16:
(7*1)+(6*3)+(5*0)+(4*5)+(3*8)+(2*1)+(1*6)=77
77 % 10 = 7
So 13058-16-7 is a valid CAS Registry Number.
InChI:InChI=1/C19H18N2O4/c22-18(23)17(10-14-11-20-16-9-5-4-8-15(14)16)21-19(24)25-12-13-6-2-1-3-7-13/h1-9,11,17,20H,10,12H2,(H,21,24)(H,22,23)

13058-16-7 Well-known Company Product Price

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  • TCI America

  • (C0641)  N-Carbobenzoxy-DL-tryptophan  >97.0%(T)

  • 13058-16-7

  • 1g

  • 210.00CNY

  • Detail
  • TCI America

  • (C0641)  N-Carbobenzoxy-DL-tryptophan  >97.0%(T)

  • 13058-16-7

  • 5g

  • 590.00CNY

  • Detail

13058-16-7SDS

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 N-Cbz-DL-Tryptophan

1.2 Other means of identification

Product number -
Other names 3-(1H-indol-3-yl)-2-(phenylmethoxycarbonylamino)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:13058-16-7 SDS

13058-16-7Relevant articles and documents

Lavendamycin analogues and methods of synthesizing and using lavendamycin analogues

-

Page/Page column 13, (2010/10/20)

Lavendamycin analogues, methods for their synthesis, and methods for their use in the treatment of diseases such as cancer and HIV infection are described.

Design and synthesis of a targeted set of aromatic amino acid derivatives for identification of new lead compounds.

Horwell,Kneen,Pritchard,Ratcliffe,Roberts,Suman-Chauhan,Steiner,Betche

, p. 1957 - 1962 (2007/10/03)

A targeted set of 256 aromatic α-amino acid derivatives is described to provide new lead compounds for biological screening. The utility is exemplified by identification of ligands for the human neuromedin B (hNMB) receptor, such as compound 3 (Ki hNMB 37nM).

Composition containing a penem or carbapenem antibiotic

-

, (2008/06/13)

Administration of an N-acylated amino acid in association with a penem or carbapenem antibiotic relieves or eliminates the renal problems associated with administration of the antibiotic alone. The amino acid derivative and antibiotic may be formulated together as a composition or administered separately, either simultaneously or sequentially. The composition may be prepared by simple mixing.

3-ACYL- AND 3-ALKOXYCARBONYL-2-OXAZOLONES AND THEIR HOMOPOLYMERS AS AMINO-PROTECTING REAGENTS

Kunieda, Takehisa,Higuchi, Tsunehiko,Abe, Yoshihiro,Hirobe, Masaaki

, p. 3065 - 3066 (2007/10/02)

3-Acyl and 3-alkoxycarbonyl-2-oxazolones as well as their homopolymers serve as practically usefull N-protecting reagents of amines including α-amino acids.

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