Welcome to LookChem.com Sign In|Join Free

CAS

  • or

155534-53-5

Post Buying Request

155534-53-5 Suppliers

Recommended suppliersmore

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

155534-53-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 155534-53-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,5,5,3 and 4 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 155534-53:
(8*1)+(7*5)+(6*5)+(5*5)+(4*3)+(3*4)+(2*5)+(1*3)=135
135 % 10 = 5
So 155534-53-5 is a valid CAS Registry Number.

155534-53-5SDS

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 2-(benzenesulfonylmethyl)-5-nitrobenzaldehyde

1.2 Other means of identification

Product number -
Other names Benzaldehyde,5-nitro-2-[(phenylsulfonyl)methyl]

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:155534-53-5 SDS

155534-53-5Relevant articles and documents

Photophysics and biological applications of the environment-sensitive fluorophore 6-N,N-dimethylamino-2,3-naphthalimide

Vazquez, M. Eugenio,Blanco, Juan B.,Imperiali

, p. 1300 - 1306 (2005)

We have synthesized a new environment-sensitive fluorophore, 6-N,N-dimethylamino-2,3-naphthalimide (6DMN). This chromophore exhibits valuable fluorescent properties as a biological probe with emission in the 500-600 nm range and a marked response to changes in the environment polarity. The 6DMN fluorescence is red-shifted in polar protic environments, with the maximum emission intensity shifting more than 100 nm from 491 nm in toluene to 592 nm in water. Additionally, the fluorescence quantum yield decreases more than 100-fold from chloroform (Φ = 0.225) to water (Φ = 0.002). The scope and applications of the 6DMN probe are expanded with the synthesis of an Fmoc-protected amino acid derivative (5), which contains the fluorophore. This unnatural amino acid has been introduced into several peptides, demonstrating that it can be manipulated under standard solid-phase peptide synthesis conditions. Peptides incorporating the new residue can be implemented for monitoring protein-protein interactions as exemplified in studies with Src homology 2 (SH2) phosphotyrosine binding domains. The designed peptides exhibit a significant increase in the quantum yield of the long wavelength fluorescence emission band (596 nm) upon binding to selected SH2 domains (e.g., Crk SH2, AbI SH2, and PI3K SH2). The peptides can be used as ratiometric sensors, since the short wavelength band (460 nm) was found almost invariable throughout the titrations.

Simple synthesis of 2-nitronaphthalene derivatives from substituted p- nitrobenzyl sulfones

Tyrala,Makosza

, p. 264 - 266 (2007/10/02)

Condensation of p-nitrobenzyl sulfones containing carbonyl or cyano substituents ortho to the methylsulfonyl group with electrophilic alkenes or alkynes as Michael acceptors provides facile and efficient access to substituted 2-nitronaphthalene derivative

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

What can I do for you?
Get Best Price

Get Best Price for 155534-53-5