Welcome to LookChem.com Sign In|Join Free

CAS

  • or

107264-05-1

Post Buying Request

107264-05-1 Suppliers

Recommended suppliersmore

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

107264-05-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 107264-05-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,2,6 and 4 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 107264-05:
(8*1)+(7*0)+(6*7)+(5*2)+(4*6)+(3*4)+(2*0)+(1*5)=101
101 % 10 = 1
So 107264-05-1 is a valid CAS Registry Number.

107264-05-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,5-dichloro-N-fluoropyridinium

1.2 Other means of identification

Product number -
Other names 3,5-Dichloro-1-fluoro-pyridinium

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:107264-05-1 SDS

107264-05-1Upstream product

107264-05-1Downstream Products

107264-05-1Relevant articles and documents

Time-resolved Spectroscopy and Charge-transfer Photochemistry of Aromatic EDA Complexes with X-Pyridinium Cations

Bockman, T. M.,Lee, K. Y.,Kochi, J. K.

, p. 1581 - 1594 (2007/10/02)

Direct photoexcitation of 1: 1 aromatic EDA complexes with various N-substituted X-pyridinium cations (X = nitro, fluoro, methoxy and acetoxy) is achieved by the specific irradiation of their charge-transfer (CT) absorption bands.Time-resolved picosecond spectroscopy refers to charge-transfer activation by the identification of the aromatic cation radical as the initial transient (T1) formed in a photoinduced electron-transfer together with the X-pyridinyl radical.The homolytic fragmentation of the latter varies with the X-substituent in the order X = NO2 > F > AcO >CH3O, and the addition of X. to the aromatic donors leads to a series of cyclohexadienyl adducts that are identified as longer-lived transients (T2) by time-resolved (nanosecond/microsecond) spectroscopy.The phototransients T1 and T2 together account for the different types of aromatic product (resulting from ring substitution, side-chain substitution and dimerization) that are generated by steady-state CT photochemistry of the aromatic EDA complexes with X-pyridinium cations.

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 107264-05-1