Welcome to LookChem.com Sign In|Join Free
  • or
N-(2,3,5,6,8,9,11,12-octahydro-1,4,7,10,13-benzopentaoxacyclopentadecin-15-yl)-acetamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

77001-48-0

Post Buying Request

77001-48-0 Suppliers

Recommended suppliers

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

77001-48-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 77001-48-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,0,0 and 1 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 77001-48:
(7*7)+(6*7)+(5*0)+(4*0)+(3*1)+(2*4)+(1*8)=110
110 % 10 = 0
So 77001-48-0 is a valid CAS Registry Number.

77001-48-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(2,3,5,6,8,9,11,12-octahydro-1,4,7,10,13-benzopentaoxacyclopentadecin-15-yl)-acetamide

1.2 Other means of identification

Product number -
Other names 15-(Acetylamino)benzo[15]krone-5

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:77001-48-0 SDS

77001-48-0Relevant academic research and scientific papers

Photochemistry of Host-Guest Complex.III. Effect of Guest Cation on the Photoreactivity of Acetophenone Oxime Derivatives Having Crown Ether Moiety

Tada, Masaru,Hirano, Hideki,Suzuki, Atsushi

, p. 2304 - 2308 (1980)

The syn-anti isomerisation of acetylbenzocrown ether oximes was stimulated by the complex-formation with sodium ion.The photolysis of these oximes gave mother ketones and amides through an oxaziridine intermediate.The photolysis of the oximes was depressed by the formation of host-guest complexes.Reactivity in the photolysis of the crown ether oximes corresponds to that 3,4-dimethoxyacetophenone oxime, whereas the reactivity of the complexed crown ether oxime with sodium ion corresponds to that of p-cyanoacetophenone oxime.Such behavior is explained by the change of the electronic properties of excited states of acetophenone oxime chromophore, which enhances the intersystem crossing.

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 77001-48-0