Welcome to LookChem.com Sign In|Join Free
  • or
BOC-CYS(BZL)-ONP is a chemical compound that features a cysteine residue (CYS) protected by a tert-butoxycarbonyl (BOC) group, a benzyl (BZL) side chain, and an o-nitrophenyl (ONP) group. It is widely utilized in biochemical and pharmaceutical research as a substrate for investigating enzymatic reactions, especially those involving cysteine proteases. The BOC protecting group shields the molecule from unwanted interactions, while the ONP group acts as a chromogenic reporter for the detection and quantification of enzymatic activity. The benzyl side chain modulates the compound's reactivity and selectivity in enzymatic reactions. BOC-CYS(BZL)-ONP is instrumental in elucidating the mechanisms and regulation of cysteine proteases, which play roles in various physiological and pathological processes.

3560-17-6

Post Buying Request

3560-17-6 Suppliers

Recommended suppliers

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

3560-17-6 Usage

Uses

Used in Biochemical Research:
BOC-CYS(BZL)-ONP is used as a substrate for studying enzymatic reactions, particularly those involving cysteine proteases, for its ability to provide insights into the mechanisms and regulation of these enzymes.
Used in Pharmaceutical Research:
BOC-CYS(BZL)-ONP is used as a tool in drug discovery and development, aiding in the identification and optimization of potential therapeutic agents targeting cysteine proteases, which are implicated in numerous diseases.
Used in Analytical Chemistry:
BOC-CYS(BZL)-ONP is used as a chromogenic reporter for the detection and measurement of enzymatic activity, providing a means to assess the efficiency and specificity of enzymatic reactions in a research setting.
Used in the Development of Diagnostic Tools:
BOC-CYS(BZL)-ONP can be employed in the creation of diagnostic assays to monitor the activity of cysteine proteases, which may serve as biomarkers for certain diseases or conditions.
Used in the Study of Physiological and Pathological Processes:
BOC-CYS(BZL)-ONP is used to investigate the role of cysteine proteases in various biological processes, contributing to a better understanding of their function in health and disease.

Check Digit Verification of cas no

The CAS Registry Mumber 3560-17-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,6 and 0 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3560-17:
(6*3)+(5*5)+(4*6)+(3*0)+(2*1)+(1*7)=76
76 % 10 = 6
So 3560-17-6 is a valid CAS Registry Number.
InChI:InChI=1/C21H24N2O6S/c1-21(2,3)29-20(25)22-18(14-30-13-15-7-5-4-6-8-15)19(24)28-17-11-9-16(10-12-17)23(26)27/h4-12,18H,13-14H2,1-3H3,(H,22,25)

3560-17-6SDS

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 BOC-CYS(BZL)-ONP

1.2 Other means of identification

Product number -
Other names BOC-S-BENZYL-L-CYSTEINE P-NITROPHENYL ESTER

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:3560-17-6 SDS

3560-17-6Relevant academic research and scientific papers

ACTIVATION OF A CARBOXY GROUP BY DIALKYL PYROCARBONATES. SYNTHESIS OF SYMMETRICAL ANHYDRIDES AND ARYL ESTERS OF N-PROTECTED AMINO ACIDS USING DI-tert-BUTYL PYROCARBONATE AS CONDENSING REAGENT

Pozdnev, V. F.,Chernaya, M. Yu.

, p. 333 - 337 (2007/10/02)

It has been shown that di-tert-butyl pyrocarbonate can be used as a condensing reagent in the production of anhydrides and some aryl esters of carboxylic acids.The synthesis of anhydrides and of phenyl, p-nitrophenyl, β-naphtyl, and quinolin-8-yl esters of N-protected amino acids is described.

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 3560-17-6