Welcome to LookChem.com Sign In|Join Free
  • or
2-Nitrophenyl N-[(benzyloxy)carbonyl]glycinate is a complex organic chemical compound with the molecular formula C16H14N2O6. It is a derivative of glycine, an amino acid, and features a nitrophenyl group and a benzyloxycarbonyl (Z) protecting group. 2-nitrophenyl N-[(benzyloxy)carbonyl]glycinate is often used in peptide synthesis as a protected amino acid, where the Z group serves to mask the amino group, preventing unwanted side reactions during the assembly of peptide chains. The nitro group on the phenyl ring provides additional reactivity and can be used in various chemical transformations. The compound is typically synthesized through the reaction of glycine with benzyl chloroformate and 2-nitrophenol, and it plays a crucial role in the field of medicinal chemistry and drug development due to its ability to form stable intermediates in the synthesis of biologically active peptides.

6154-41-2

Post Buying Request

6154-41-2 Suppliers

Recommended suppliers

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

6154-41-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6154-41-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,5 and 4 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6154-41:
(6*6)+(5*1)+(4*5)+(3*4)+(2*4)+(1*1)=82
82 % 10 = 2
So 6154-41-2 is a valid CAS Registry Number.

6154-41-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (2-nitrophenyl) 2-(phenylmethoxycarbonylamino)acetate

1.2 Other means of identification

Product number -
Other names Z-Gly-O-o-nitrophenylester

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:6154-41-2 SDS

6154-41-2Relevant academic research and scientific papers

Ph3P-I2 mediated aryl esterification with a mechanistic insight

Phakhodee, Wong,Duangkamol, Chuthamat,Pattarawarapan, Mookda

supporting information, p. 2087 - 2089 (2016/04/26)

In order to better understand the reaction mechanism and to obtain optimal conditions, the Ph3P-I2/Et3N mediated aryl esterification reaction was thoroughly investigated. Using a specific reagent addition sequence, the reaction proceeds remarkably well especially with acidic substrates. 31P NMR studies revealed that the formation of an aryloxyphosphonium salt is crucial in governing the reaction path toward the formation of phenolic esters.

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 6154-41-2