Welcome to LookChem.com Sign In|Join Free
  • or
N-(6-CHLOROHEXYL)PHTHALIMIDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

70466-03-4

Post Buying Request

70466-03-4 Suppliers

Recommended suppliers

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

70466-03-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 70466-03-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,4,6 and 6 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 70466-03:
(7*7)+(6*0)+(5*4)+(4*6)+(3*6)+(2*0)+(1*3)=114
114 % 10 = 4
So 70466-03-4 is a valid CAS Registry Number.

70466-03-4SDS

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 2-(6-chlorohexyl)isoindole-1,3-dione

1.2 Other means of identification

Product number -
Other names N-(6-CHLOROHEXYL)PHTHALIMIDE

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:70466-03-4 SDS

70466-03-4Downstream Products

70466-03-4Relevant academic research and scientific papers

Catalytic remote hydrohalogenation of internal alkenes

Chen, Pinhong,Jin, Jianbo,Li, Xiang,Liu, Guosheng

, (2022/02/07)

Primary alkyl halides have broad utility as fine chemicals in organic synthesis. The direct halogenation of alkenes is one of the most efficient approaches for the synthesis of these halides. Internal alkenes, in particular mixtures of isomers from refine

Synthesis of lariat diazacrown ethers with terminal amino groups in the side chains

Lukyanenko,Kirichenko,Shcherbakov

, p. 343 - 350 (2007/10/03)

Treatment of diazacrown ethers with N-(haloalkyl)- and N-(haloethoxy) phthalimides gives the corresponding N,N′- substituted diazacrown ether. Hydrazinolysis of the latter then gives diazacrown ethers with terminal primary amino groups in the side chain. Their reductive methylation using formaldehyde in formic acid gives the dimethylamino derivatives. The presence of a lariat effect was demonstrated by treating the compounds obtained with picrates of alkali and alkaline-earth metals.

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 70466-03-4