Welcome to LookChem.com Sign In|Join Free
  • or
N-butyl-2,6-dioxo-1,2,3,6-tetrahydropyrimidine-4-carboxamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

13156-38-2

Post Buying Request

13156-38-2 Suppliers

Recommended suppliers

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

13156-38-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13156-38-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,1,5 and 6 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 13156-38:
(7*1)+(6*3)+(5*1)+(4*5)+(3*6)+(2*3)+(1*8)=82
82 % 10 = 2
So 13156-38-2 is a valid CAS Registry Number.

13156-38-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name N-butyl-2,6-dioxo-3H-pyrimidine-4-carboxamide

1.2 Other means of identification

Product number -
Other names 2,6-Dioxo-1,2,3,6-tetrahydro-pyrimidin-4-carbonsaeure-amid

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:13156-38-2 SDS

13156-38-2Downstream Products

13156-38-2Relevant academic research and scientific papers

Synthesis of substituted pyrimidine hydrazine acids (PHA) and their use in peptide recognition

Miltschitzky, Stefan,Michlova, Veronika,Stadlbauer, Stefan,Koenig, Burkhard

, p. 135 - 160 (2007/10/03)

Substituted pyrimidine-hydrazine-acids (PHA) were prepared from orotic acid in five synthetic steps and high yields. Their geometry of hydrogen bond acceptor and donor sites make them suitable for the molecular recognition of peptide β-sheets. In non-protic solvents the PHA unit emits at around 420 nm after irradiation at 281 nm. The emission intensity decreases upon peptide binding and signals the binding event. Peptides consisting of PHAs and natural amino acids or a turn structure motif were prepared. The investigation of the intramolecular binding pattern by NMR spectroscopy revealed the expected interaction of the PHA and peptide β-sheet.

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 13156-38-2