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35761-26-3

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35761-26-3 Usage

Chemical Properties

White Solid

Uses

Different sources of media describe the Uses of 35761-26-3 differently. You can refer to the following data:
1. Nalpha-Benzyloxycarbonyl-L-2,3-diaminopropionic acid is a important building block for the synthesis of peptides containing DAP residues, e.g. bleomycins, edeines, tuberactinomycins.
2. Important building block for the synthesis of peptides containing DAP residues, e.g. bleomycins, edeines, tuberactinomycins

Check Digit Verification of cas no

The CAS Registry Mumber 35761-26-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,7,6 and 1 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 35761-26:
(7*3)+(6*5)+(5*7)+(4*6)+(3*1)+(2*2)+(1*6)=123
123 % 10 = 3
So 35761-26-3 is a valid CAS Registry Number.
InChI:InChI=1/C11H14N2O4/c12-9(10(14)15)6-13-11(16)17-7-8-4-2-1-3-5-8/h1-5,9H,6-7,12H2,(H,13,16)(H,14,15)

35761-26-3 Well-known Company Product Price

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  • (Code)Product description
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  • Detail
  • TCI America

  • (A2471)  (S)-3-Amino-2-(carbobenzoxyamino)propionic Acid  >98.0%(HPLC)(T)

  • 35761-26-3

  • 1g

  • 580.00CNY

  • Detail
  • TCI America

  • (A2471)  (S)-3-Amino-2-(carbobenzoxyamino)propionic Acid  >98.0%(HPLC)(T)

  • 35761-26-3

  • 5g

  • 1,650.00CNY

  • Detail
  • Alfa Aesar

  • (H62025)  Nalpha-Benzyloxycarbonyl-L-2,3-diaminopropionic acid, 98%   

  • 35761-26-3

  • 1g

  • 1049.0CNY

  • Detail
  • Alfa Aesar

  • (H62025)  Nalpha-Benzyloxycarbonyl-L-2,3-diaminopropionic acid, 98%   

  • 35761-26-3

  • 5g

  • 4724.0CNY

  • Detail
  • Aldrich

  • (96085)  Z-Dap-OH  ≥98.0% (NT)

  • 35761-26-3

  • 96085-5G

  • 7,058.61CNY

  • Detail

35761-26-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name (S)-3-Amino-2-(benzyloxycarbonylamino)-propanoic acid

1.2 Other means of identification

Product number -
Other names 3-Amino-N-Cbz-L-alanine

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:35761-26-3 SDS

35761-26-3Relevant articles and documents

Functional Disruption of the Cancer-Relevant Interaction between Survivin and Histone H3 with a Guanidiniocarbonyl Pyrrole Ligand

Aschmann, Dennis,Bayer, Peter,Beuck, Christine,Ehlers, Martin,Giese, Michael,Killa, Matthias,Knauer, Shirley K.,Meiners, Annika,Mertel, Marcel,Schmuck, Carsten,Vallet, Cecilia

, p. 5567 - 5571 (2020)

The protein Survivin is highly upregulated in most cancers and considered to be a key player in carcinogenesis. We explored a supramolecular approach to address Survivin as a drug target by inhibiting the protein–protein interaction of Survivin and its fu

PYRROLOBENZODIAZEPINE DIMER PRECURSOR AND LIGAND-LINKER CONJUGATE COMPOUND THEREOF

-

, (2020/02/18)

The present invention relates to a pyrrolobenzodiazepine dimer prodrug and a ligand-linker conjugate compound thereof, a composition containing these, and therapeutic use thereof particularly as an anticancer drug. The stability of the compounds themselves and the stability thereof in plasma are excellent and the compounds are advantageous in terms of manifestation of toxicity, and thus the compounds are industrially useful in that it is possible to target proliferative diseases such as cancer, to perform a specific treatment, to maximize the drug efficacy, and to minimize the occurrence of side effects.

Phosphate bioisostere containing amphiphiles: A novel class of squaramide-based lipids

Saha, Abhishek,Panda, Subhankar,Paul, Saurav,Manna, Debasis

, p. 9438 - 9441 (2016/07/29)

We describe a novel class of amphiphiles with squaramide moiety as a phosphate bioisostere. Most synthesized squaramide-based amphiphiles have the favorable physicochemical properties of lipids, such as: formation of stable liposomes or giant unilamellar vesicles in aqueous solution, high phase-transition temperature, low vesicle leakage and phospholipase resistance properties.

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