Welcome to LookChem.com Sign In|Join Free
  • or
N,N'-bis-phenylcarbamoyl-L-cystine is a synthetic chemical compound with the molecular formula C17H18N2O4S. It is derived from the amino acid L-cystine, where two phenylcarbamoyl groups are attached to the nitrogen atoms of the cystine molecule. N.N'-bis-phenylcarbamoyl-L-cystine is often used in peptide synthesis and as a building block for the creation of more complex organic molecules. It plays a role in the formation of disulfide bonds, which are crucial for the stability and structure of proteins. The compound is also of interest in the field of materials science, particularly in the development of new polymers and materials with unique properties.

6630-89-3

Post Buying Request

6630-89-3 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

6630-89-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6630-89-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,3 and 0 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6630-89:
(6*6)+(5*6)+(4*3)+(3*0)+(2*8)+(1*9)=103
103 % 10 = 3
So 6630-89-3 is a valid CAS Registry Number.

6630-89-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N'-bis-phenylcarbamoyl-cystine

1.2 Other means of identification

Product number -
Other names N,N'-Bis-phenylcarbamoyl-cystin

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:6630-89-3 SDS

6630-89-3Downstream Products

6630-89-3Relevant academic research and scientific papers

Chelate oxorhenium to assemble new integrin antagonists

Le Gal, Julien,Gonera, Marta,Lelait, Marie-Anne,Servent, Denis,Dugave, Christophe

scheme or table, p. 880 - 886 (2012/03/26)

Assembly of independent chemical modules through oxorhenium coordination by a NS2 + S chelation motif was applied to the synthesis of RGD (Arg-Gly-Asp) analogs. Modules were assembled through oxorhenium chelation to give a series of 18 metal complexes in good yields and satisfactory purities. Screening of these oxorhenium coordinates as antagonists of integrins αVβ3, αIIbβ3 and αVβ5 led to the identification of 3 bioactive compounds that exhibit submicromolar affinities for the 3 integrins. Preliminary studies showed that the corresponding oxotechnetium complexes are stable in mice plasma and therefore could be proposed for the molecular imaging of pathologies that overexpress integrins αVβ3 and αVβ5.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 6630-89-3